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    <loc>https://www.phscientific.com/products/df2718</loc>
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      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6799_thumb_P_1467071877690.jpg?v=1592397125</image:loc>
      <image:title>HOR5&apos;Beta13 Antibody</image:title>
      <image:caption>Western blot analysis of HOR5&apos;Beta13 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
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  <url>
    <loc>https://www.phscientific.com/products/df2719</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
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    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6800_thumb_P_1465347059122.jpg?v=1592397123</image:loc>
      <image:title>FPRL1 Antibody</image:title>
      <image:caption>DF2719 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
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  <url>
    <loc>https://www.phscientific.com/products/df2720</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6801_thumb_P_1465347127457.jpg?v=1592397121</image:loc>
      <image:title>GPR1 Antibody</image:title>
      <image:caption>DF2720 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
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  <url>
    <loc>https://www.phscientific.com/products/df2721</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
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    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6802_thumb_P_1465347149446.jpg?v=1592397119</image:loc>
      <image:title>GPR12 Antibody</image:title>
      <image:caption>Western blot analysis of GPR12 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2722</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6803_thumb_P_1465347175328.jpg?v=1592397118</image:loc>
      <image:title>GPR128 Antibody</image:title>
      <image:caption>DF2722 at 1/100 staining Human liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
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  <url>
    <loc>https://www.phscientific.com/products/df2723</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6804_thumb_P_1465347195159.jpg?v=1592397115</image:loc>
      <image:title>GPR133 Antibody</image:title>
      <image:caption>DF2723 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2724</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6805_thumb_P_1465347221695.jpg?v=1592397114</image:loc>
      <image:title>GPR136 Antibody</image:title>
      <image:caption>Western blot analysis of GPR136 expression in  HUVEC cell lysate ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2725</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6806_thumb_P_1465347239291.jpg?v=1592397112</image:loc>
      <image:title>GPR146 Antibody</image:title>
      <image:caption>DF2725 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2726</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6807_thumb_P_1465347258774.jpg?v=1592397110</image:loc>
      <image:title>GPR148 Antibody</image:title>
      <image:caption>DF2726 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2727</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6808_thumb_P_1465347278586.jpg?v=1592397108</image:loc>
      <image:title>GPR15 Antibody</image:title>
      <image:caption>Western blot analysis of GPR15 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2728</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6809_thumb_P_1465347295039.jpg?v=1592397106</image:loc>
      <image:title>GPR161 Antibody</image:title>
      <image:caption>DF2728 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
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  <url>
    <loc>https://www.phscientific.com/products/df2729</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6810_thumb_P_1465347318868.jpg?v=1592397104</image:loc>
      <image:title>GPR19 Antibody</image:title>
      <image:caption>Western blot analysis of GPR19 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2730</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6811_thumb_P_1465347338888.jpg?v=1592397102</image:loc>
      <image:title>GPR20 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hybridoma cells, using GPR20 Antibody. The lane on the left was treated with blocking peptide.
Observed bands: 55 kDa.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2731</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6812_thumb_P_1465347356065.jpg?v=1592397101</image:loc>
      <image:title>GPR21 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using GPR21 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2732</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6813_thumb_P_1465347372807.jpg?v=1592397099</image:loc>
      <image:title>GPR22 Antibody</image:title>
      <image:caption>Western blot analysis of GPR22 expression in  HepG2 cell line lysates ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2733</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6814_thumb_P_1465347392629.jpg?v=1592397097</image:loc>
      <image:title>GPR25 Antibody</image:title>
      <image:caption>Western blot analysis of GPR25 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2734</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6815_thumb_P_1465347418193.jpg?v=1592397095</image:loc>
      <image:title>GPR26 Antibody</image:title>
      <image:caption>Western blot analysis of GPR26 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2735</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6816_thumb_P_1465347443833.jpg?v=1592397094</image:loc>
      <image:title>GPR27 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hepg2, using GPR27 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2736</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6817_thumb_P_1465347465635.jpg?v=1592397092</image:loc>
      <image:title>GPR3 Antibody</image:title>
      <image:caption>Western blot analysis of GPR3 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2737</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6818_thumb_P_1465347483067.jpg?v=1592397090</image:loc>
      <image:title>GPR30 Antibody</image:title>
      <image:caption>Western blot analysis of GPR30 expression in ; HepG2 cell lysate,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2738</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6819_thumb_P_1465347502170.jpg?v=1592397089</image:loc>
      <image:title>GPR31 Antibody</image:title>
      <image:caption>DF2738 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2739</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6820_thumb_P_1465347518664.jpg?v=1592397087</image:loc>
      <image:title>GPR32 Antibody</image:title>
      <image:caption>DF2739 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2740</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6821_thumb_P_1465347537784.jpg?v=1592397085</image:loc>
      <image:title>GPR34 Antibody</image:title>
      <image:caption>Western blot analysis of GPR34 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2741</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6822_thumb_P_1465347556456.jpg?v=1592397083</image:loc>
      <image:title>GPR35 Antibody</image:title>
      <image:caption>Western blot analysis of GPR35 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2742</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6823_thumb_P_1465347573897.jpg?v=1592397081</image:loc>
      <image:title>GPR37 Antibody</image:title>
      <image:caption>Western blot analysis of GPR37 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2743</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6824_thumb_P_1465347607263.jpg?v=1592397080</image:loc>
      <image:title>GPR39 Antibody</image:title>
      <image:caption>DF2743 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2744</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6825_thumb_P_1465347626078.jpg?v=1592397078</image:loc>
      <image:title>GPR4 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using GPR4 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2745</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6826_thumb_P_1465347640234.jpg?v=1592397074</image:loc>
      <image:title>GPR40 Antibody</image:title>
      <image:caption>Western blot analysis of GPR40 expression in  Hela cell lysate,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2746</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6827_thumb_P_1465347662636.jpg?v=1592397072</image:loc>
      <image:title>GPR43 Antibody</image:title>
      <image:caption>DF2746 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2747</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6828_thumb_P_1465347686912.jpg?v=1592397070</image:loc>
      <image:title>GPR44 Antibody</image:title>
      <image:caption>DF2747 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2748</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6829_thumb_P_1465347719852.jpg?v=1592397069</image:loc>
      <image:title>GPR45 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using GPR45 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2749</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6830_thumb_P_1465347736223.jpg?v=1592397067</image:loc>
      <image:title>GPR48 Antibody</image:title>
      <image:caption>Western blot analysis of GPR48 expression in Jurkat cell lysate,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2750</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6831_thumb_P_1465347753093.jpg?v=1592397065</image:loc>
      <image:title>GPR52 Antibody</image:title>
      <image:caption>Western blot analysis of GPR52 expression in  Hela cell lysate,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2751</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6832_thumb_P_1465347778659.jpg?v=1592397063</image:loc>
      <image:title>GPR54 Antibody</image:title>
      <image:caption>DF2751 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2752</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6833_thumb_P_1465347854757.jpg?v=1592397062</image:loc>
      <image:title>GPR55 Antibody</image:title>
      <image:caption>DF2752 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2753</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6834_thumb_P_1465347869238.jpg?v=1592397060</image:loc>
      <image:title>GPR56 Antibody</image:title>
      <image:caption>DF2753 at 1/100 staining Human lymph node tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2754</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6835_thumb_P_1465347902831.jpg?v=1592397058</image:loc>
      <image:title>GPR6 Antibody</image:title>
      <image:caption>Western blot analysis of GPR6 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2755</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6836_thumb_P_1465347928588.jpg?v=1592397056</image:loc>
      <image:title>GPR61 Antibody</image:title>
      <image:caption>Western blot analysis of GPR61 expression in  A431 cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2756</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6837_thumb_P_1465347959283_da13e927-8f2c-49c6-9b22-a796c078ea09.jpg?v=1592397054</image:loc>
      <image:title>GPR62 Antibody</image:title>
      <image:caption></image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2757</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6838_thumb_P_1465347994223.jpg?v=1592397053</image:loc>
      <image:title>GPR63 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hybridoma cells, using GPR63 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2758</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df2758_gpr64_antibody_thumb_P_1548035685822.jpg?v=1592397051</image:loc>
      <image:title>GPR64 Antibody</image:title>
      <image:caption>Western blot analysis of GPR64 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2759</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6840_thumb_P_1465348060349.jpg?v=1592397049</image:loc>
      <image:title>GPR68 Antibody</image:title>
      <image:caption>DF2759 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2760</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6841_thumb_P_1465348087198.jpg?v=1592397048</image:loc>
      <image:title>GPR7 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Mouse brain, using GPR7 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2761</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6842_thumb_P_1465348108176.jpg?v=1592397046</image:loc>
      <image:title>GPR75 Antibody</image:title>
      <image:caption>Western blot analysis of GPR75 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2762</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6843_thumb_P_1465348128753.jpg?v=1592397044</image:loc>
      <image:title>GPR77 Antibody</image:title>
      <image:caption>DF2762 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2763</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6844_thumb_P_1465348177333.jpg?v=1592397043</image:loc>
      <image:title>GPR78 Antibody</image:title>
      <image:caption>DF2763 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2764</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6845_thumb_P_1463027711145.jpg?v=1592397041</image:loc>
      <image:title>GPR8 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using GPR8 Antibody.
 Lane 1: COS7 treated with blocking peptide;
 Lane 2: COS7;
 Lane 3: B16F10.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2765</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6846_thumb_P_1465348213400.jpg?v=1592397039</image:loc>
      <image:title>GPR80/GPR99 Antibody</image:title>
      <image:caption>Western blot analysis of GPR80/GPR99 expression in  Human placenta tissue lysates ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2766</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6847_thumb_P_1465348313448.jpg?v=1592397037</image:loc>
      <image:title>GPR81 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using GPR81 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2767</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6848_thumb_P_1465348334859.jpg?v=1592397036</image:loc>
      <image:title>GPR82 Antibody</image:title>
      <image:caption>Western blot analysis of GPR82 expression in  A549 whole cell lysates ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2768</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6849_thumb_P_1465348354378.jpg?v=1592397034</image:loc>
      <image:title>GPR83/GPR72 Antibody</image:title>
      <image:caption>Western blot analysis of GPR83/GPR72 expression in  Rat brain lysates in RIPA buffer ;developed using the ECL technique;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2769</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6850_thumb_P_1465348389110.jpg?v=1592397032</image:loc>
      <image:title>GPR84 Antibody</image:title>
      <image:caption>DF2769 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2770</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6851_thumb_P_1465348411295.jpg?v=1592397031</image:loc>
      <image:title>GPR86/GPR94 Antibody</image:title>
      <image:caption>DF2770 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2771</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6852_thumb_P_1465348432225.jpg?v=1592397029</image:loc>
      <image:title>GPR87/GPR95 Antibody</image:title>
      <image:caption>Western blot analysis of GPR87/GPR95 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2772</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6853_thumb_P_1465348456834.jpg?v=1592397027</image:loc>
      <image:title>GPR89A Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using GPR89A Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2773</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6854_thumb_P_1465348476170.jpg?v=1592397025</image:loc>
      <image:title>GPR91 Antibody</image:title>
      <image:caption>DF2773 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2774</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6855_thumb_P_1465348496818.jpg?v=1592397023</image:loc>
      <image:title>GPR92/GPR93 Antibody</image:title>
      <image:caption>DF2774 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2775</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6856_thumb_P_1465348560928.jpg?v=1592397021</image:loc>
      <image:title>GPR97 Antibody</image:title>
      <image:caption>DF2775 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2776</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6857_thumb_P_1465348583029.jpg?v=1592397020</image:loc>
      <image:title>EBI2 Antibody</image:title>
      <image:caption>DF2776 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2777</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6858_thumb_P_1465348633455.jpg?v=1592397018</image:loc>
      <image:title>SS2R Antibody</image:title>
      <image:caption>Western blot analysis of SS2R expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2778</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6859_thumb_P_1465348679661.jpg?v=1592397016</image:loc>
      <image:title>SS3R Antibody</image:title>
      <image:caption>DF2778 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2779</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6860_thumb_P_1465348724944.jpg?v=1592397014</image:loc>
      <image:title>SS4R Antibody</image:title>
      <image:caption>DF2779 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2780</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6861_thumb_P_1465348752076.jpg?v=1592397012</image:loc>
      <image:title>SS5R Antibody</image:title>
      <image:caption>DF2780 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2781</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6862_thumb_P_1465348770515.jpg?v=1592397011</image:loc>
      <image:title>CHRM3 Antibody</image:title>
      <image:caption>Western blot analysis of CHRM3 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2782</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6863_thumb_P_1465348805934.jpg?v=1592397009</image:loc>
      <image:title>C5ARL Antibody</image:title>
      <image:caption>DF2782 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2783</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6864_thumb_P_1465348826604.jpg?v=1592397007</image:loc>
      <image:title>CXCR2 Antibody</image:title>
      <image:caption>DF2783 at 1/100 staining human Lymphoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2784</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6865_thumb_P_1465348882911.jpg?v=1592397006</image:loc>
      <image:title>EBI2 Antibody</image:title>
      <image:caption>Western blot analysis of EBI2 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2785</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6866_thumb_P_1465348903109.jpg?v=1592397004</image:loc>
      <image:title>EDG1 Antibody</image:title>
      <image:caption>DF2785 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2786</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6867_thumb_P_1465348947092.jpg?v=1592397002</image:loc>
      <image:title>EDG2 Antibody</image:title>
      <image:caption>DF2786 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2787</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6868_thumb_P_1465348965369.jpg?v=1592397000</image:loc>
      <image:title>EDG8 Antibody</image:title>
      <image:caption>Western blot analysis of EDG8 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2788</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6869_thumb_P_1465348988013.jpg?v=1592396999</image:loc>
      <image:title>EDNRB Antibody</image:title>
      <image:caption>DF2788 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600 was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2789</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6870_thumb_P_1465349006585.jpg?v=1592396997</image:loc>
      <image:title>EMR1 Antibody</image:title>
      <image:caption>Western blot analysis of EMR1 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2790</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6871_thumb_P_1465349025008.jpg?v=1592396995</image:loc>
      <image:title>FZD10 Antibody</image:title>
      <image:caption>DF2790 staining COS7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2791</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6872_thumb_P_1465349047078.jpg?v=1592396993</image:loc>
      <image:title>FZD2 Antibody</image:title>
      <image:caption>DF2791 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2792</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6873_thumb_P_1465349067526.jpg?v=1592396991</image:loc>
      <image:title>GPR137B Antibody</image:title>
      <image:caption>Western blot analysis of GPR137B expression in  HepG2 cell lysate ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2793</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6874_thumb_P_1465349089074.jpg?v=1592396982</image:loc>
      <image:title>GASR Antibody</image:title>
      <image:caption>DF2793 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2794</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6875_thumb_P_1465349107223.jpg?v=1592396980</image:loc>
      <image:title>GHSR Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using GHSR Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2795</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6876_thumb_P_1465349124428.jpg?v=1592396979</image:loc>
      <image:title>GNRHR2 Antibody</image:title>
      <image:caption>DF2795 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2796</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6877_thumb_P_1465349146349.jpg?v=1592396977</image:loc>
      <image:title>GPR110 Antibody</image:title>
      <image:caption>DF2796 at 1/100 staining Mouse kidney tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2797</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6878_thumb_P_1465349170227.jpg?v=1592396975</image:loc>
      <image:title>GPR141 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using GPR141 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2798</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6879_thumb_P_1465349197147.jpg?v=1592396973</image:loc>
      <image:title>GPR161 Antibody</image:title>
      <image:caption>DF2798 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2799</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6880_thumb_P_1465349233020.jpg?v=1592396971</image:loc>
      <image:title>GPR162 Antibody</image:title>
      <image:caption>Western blot analysis of GPR162 Antibody expression in A431 cells lysates.The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2800</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6881_thumb_P_1465349278473.jpg?v=1592396970</image:loc>
      <image:title>GPR176 Antibody</image:title>
      <image:caption>DF2800 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2801</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6882_thumb_P_1465349307438.jpg?v=1592396968</image:loc>
      <image:title>GPR1 Antibody</image:title>
      <image:caption>Western blot analysis of GPR1 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2802</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6883_thumb_P_1465349340226.jpg?v=1592396966</image:loc>
      <image:title>GPR21 Antibody</image:title>
      <image:caption>Western blot analysis of GPR21 expression in  HT1080 whole cell lysate ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2803</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6884_thumb_P_1465349473141.jpg?v=1592396964</image:loc>
      <image:title>GPR26 Antibody</image:title>
      <image:caption>Western blot analysis of GPR26 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2804</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df2804_gpr33_antibody_thumb_P_1549895529591.jpg?v=1592396963</image:loc>
      <image:title>GPR33 Antibody</image:title>
      <image:caption>DF2804 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2805</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6886_thumb_P_1465349643251.jpg?v=1592396961</image:loc>
      <image:title>GPR39 Antibody</image:title>
      <image:caption>DF2805 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2806</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6887_thumb_P_1465349663970.jpg?v=1592396959</image:loc>
      <image:title>GPR4 Antibody</image:title>
      <image:caption>Western blot analysis of GPR4 expression in  Raji whole cell lysate ;;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2807</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6888_thumb_P_1465349699225.jpg?v=1592396957</image:loc>
      <image:title>GPR44 Antibody</image:title>
      <image:caption>Western blot analysis of GPR44 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2808</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6889_thumb_P_1465349724696.jpg?v=1592396956</image:loc>
      <image:title>GPR45 Antibody</image:title>
      <image:caption>Western blot analysis of GPR45 expression in  RPMI-8226 whole cell lysate ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2809</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6890_thumb_P_1465349751241.jpg?v=1592396954</image:loc>
      <image:title>GPR55 Antibody</image:title>
      <image:caption>DF2809 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2810</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6891_thumb_P_1465349783013.jpg?v=1592396952</image:loc>
      <image:title>GPR61 Antibody</image:title>
      <image:caption>Western blot analysis of GPR61 expression in  A431 cell lysate ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2811</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6892_thumb_P_1465349801084.jpg?v=1592396950</image:loc>
      <image:title>GPR84 Antibody</image:title>
      <image:caption>DF2811 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2812</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6893_thumb_P_1465349873378.jpg?v=1592396948</image:loc>
      <image:title>GPR88 Antibody</image:title>
      <image:caption>Western blot analysis of GPR88 expression in  Rat brain lysate ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2813</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6894_thumb_P_1465349895575.jpg?v=1592396947</image:loc>
      <image:title>GPR97 Antibody</image:title>
      <image:caption>DF2813 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2814</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6895_thumb_P_1465349923160.jpg?v=1592396945</image:loc>
      <image:title>GRM6 Antibody</image:title>
      <image:caption>Western blot analysis of GRM6 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2815</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6896_thumb_P_1465349959510.jpg?v=1592396943</image:loc>
      <image:title>GRPR Antibody</image:title>
      <image:caption>Western blot analysis of GRPR expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2816</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6897_thumb_P_1465349979767.jpg?v=1592396941</image:loc>
      <image:title>LGR5 Antibody</image:title>
      <image:caption>DF2816 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2817</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6898_thumb_P_1465350016941.jpg?v=1592396940</image:loc>
      <image:title>LPHN3 Antibody</image:title>
      <image:caption>Western blot analysis of LPHN3 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2818</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2819</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6900_thumb_P_1465350063674.jpg?v=1592396937</image:loc>
      <image:title>MCHR1 Antibody</image:title>
      <image:caption>Western blot analysis of MCHR1 expression in  IMR32 whole cell lysate ;,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2820</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6901_thumb_P_1465350089489.jpg?v=1592396935</image:loc>
      <image:title>MRGRD Antibody</image:title>
      <image:caption>DF2820 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2821</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6902_thumb_P_1465350109971.jpg?v=1592396933</image:loc>
      <image:title>NMUR2 Antibody</image:title>
      <image:caption>DF2821 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2822</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6903_thumb_P_1465350134103.jpg?v=1592396931</image:loc>
      <image:title>NPSR1 Antibody</image:title>
      <image:caption>Western blot analysis of NPSR1 expression in HEK293 cells ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2823</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6904_thumb_P_1465350157453.jpg?v=1592396929</image:loc>
      <image:title>NPY4R Antibody</image:title>
      <image:caption>DF2823 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2824</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6905_thumb_P_1465350176724.jpg?v=1592396927</image:loc>
      <image:title>OR2A12 Antibody</image:title>
      <image:caption>DF2824 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2825</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6906_thumb_P_1465350201534.jpg?v=1592396925</image:loc>
      <image:title>OR2T8/2T12/2T33 Antibody</image:title>
      <image:caption>DF2825 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2826</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6907_thumb_P_1465350219278.jpg?v=1592396923</image:loc>
      <image:title>OR4C45 Antibody</image:title>
      <image:caption>DF2826 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2827</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6908_thumb_P_1465350243912.jpg?v=1592396921</image:loc>
      <image:title>OR4F3/4F21 Antibody</image:title>
      <image:caption>DF2827 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2828</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6909_thumb_P_1465350267401.jpg?v=1592396919</image:loc>
      <image:title>OR51L1 Antibody</image:title>
      <image:caption>DF2828 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2829</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6910_thumb_P_1465350288840.jpg?v=1592396918</image:loc>
      <image:title>OR51M1 Antibody</image:title>
      <image:caption>DF2829 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2830</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6911_thumb_P_1465350332464.jpg?v=1592396916</image:loc>
      <image:title>OR5AN1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using OR5AN1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2831</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6912_thumb_P_1465350356847.jpg?v=1592396914</image:loc>
      <image:title>OR5H6/5H14 Antibody</image:title>
      <image:caption>DF2831 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2832</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6913_thumb_P_1465350376402.jpg?v=1592396912</image:loc>
      <image:title>OR6C75 Antibody</image:title>
      <image:caption>DF2832 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2833</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6914_thumb_P_1465350398737.jpg?v=1592396910</image:loc>
      <image:title>OR7E24 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Mouse brain, using OR7E24 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2834</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6915_thumb_P_1465350439293.jpg?v=1592396909</image:loc>
      <image:title>OPRL1 Antibody</image:title>
      <image:caption>Western blot analysis of OPRL1 expression in A431 whole cell lysate ,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2835</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6916_thumb_P_1467071890134.jpg?v=1592396907</image:loc>
      <image:title>OR10Q1 Antibody</image:title>
      <image:caption>DF2835 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2836</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6917_thumb_P_1465350633125.jpg?v=1592396905</image:loc>
      <image:title>OR1F1 Antibody</image:title>
      <image:caption>DF2836 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2837</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6918_thumb_P_1467071908427.jpg?v=1592396904</image:loc>
      <image:title>OR1G1 Antibody</image:title>
      <image:caption>DF2837 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2838</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6919_thumb_P_1465350702841.jpg?v=1592396902</image:loc>
      <image:title>OR1I1 Antibody</image:title>
      <image:caption>DF2838 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2839</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6920_thumb_P_1467071938857.jpg?v=1592396900</image:loc>
      <image:title>OR1J1 Antibody</image:title>
      <image:caption>DF2839 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2840</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6921_thumb_P_1465351051885.jpg?v=1592396898</image:loc>
      <image:title>OR1J4 Antibody</image:title>
      <image:caption>DF2840 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2841</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6922_thumb_P_1465351088590.jpg?v=1592396896</image:loc>
      <image:title>OR1J2/1N2 Antibody</image:title>
      <image:caption>DF2841 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2842</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6923_thumb_P_1465351130992.jpg?v=1592396891</image:loc>
      <image:title>OR1L1 Antibody</image:title>
      <image:caption>DF2842 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2843</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6924_thumb_P_1465351151845.jpg?v=1592396889</image:loc>
      <image:title>OR1L3 Antibody</image:title>
      <image:caption>DF2843 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2844</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6925_thumb_P_1465351173264.jpg?v=1592396887</image:loc>
      <image:title>OR1L4/1L6 Antibody</image:title>
      <image:caption>DF2844 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2845</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6926_thumb_P_1465351199717.jpg?v=1592396886</image:loc>
      <image:title>OR2A12 Antibody</image:title>
      <image:caption>DF2845 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2846</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6927_thumb_P_1467071965714.jpg?v=1592396884</image:loc>
      <image:title>OR2A2 Antibody</image:title>
      <image:caption>DF2846 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2847</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6928_thumb_P_1467071987583.jpg?v=1592396882</image:loc>
      <image:title>OR2H1 Antibody</image:title>
      <image:caption>DF2847 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2848</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6929_thumb_P_1467072012523.jpg?v=1592396880</image:loc>
      <image:title>OR2L3/2L8 Antibody</image:title>
      <image:caption>DF2848 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2849</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6930_thumb_P_1467072042595.jpg?v=1592396879</image:loc>
      <image:title>OR2L3/2L8 Antibody</image:title>
      <image:caption>DF2849 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2850</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6931_thumb_P_1465351294521.jpg?v=1592396877</image:loc>
      <image:title>OR2M4 Antibody</image:title>
      <image:caption>DF2850 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2851</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6932_thumb_P_1465351324470.jpg?v=1592396875</image:loc>
      <image:title>OR2S2 Antibody</image:title>
      <image:caption>DF2851 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2852</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df2852_or2t27_antibody_thumb_P_1549895529421.jpg?v=1592396873</image:loc>
      <image:title>OR2T27 Antibody</image:title>
      <image:caption>DF2852 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2853</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6934_thumb_P_1465351354711.jpg?v=1592396871</image:loc>
      <image:title>OR2T6 Antibody</image:title>
      <image:caption>DF2853 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2854</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6935_thumb_P_1467072061813.jpg?v=1592396870</image:loc>
      <image:title>OR2V1 Antibody</image:title>
      <image:caption>DF2854 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2855</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6936_thumb_P_1465351373334.jpg?v=1592396868</image:loc>
      <image:title>OR2V2 Antibody</image:title>
      <image:caption>DF2855 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2856</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6937_thumb_P_1465351409031.jpg?v=1592396867</image:loc>
      <image:title>OR2W1 Antibody</image:title>
      <image:caption>DF2856 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2857</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6938_thumb_P_1465351439784.jpg?v=1592396865</image:loc>
      <image:title>OR3A1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using OR3A1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2858</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6939_thumb_P_1465351457022.jpg?v=1592396863</image:loc>
      <image:title>RGR Antibody</image:title>
      <image:caption>DF2858 at 1/100 staining Human Head and neck cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2859</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/6940_thumb_P_1467072117297.jpg?v=1592396861</image:loc>
      <image:title>PJCG2 Antibody</image:title>
      <image:caption>HL-60 cell lysate</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2900</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11153_thumb_P_1465351480626.jpg?v=1592396860</image:loc>
      <image:title>Alas1 Antibody</image:title>
      <image:caption>DF2900 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2901</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11154_thumb_P_1465351499328.jpg?v=1592396858</image:loc>
      <image:title>alpha Tubulin 4A Antibody</image:title>
      <image:caption>DF2901 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2902</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11155_thumb_P_1465351514862.jpg?v=1592396856</image:loc>
      <image:title>ARRB1 Antibody</image:title>
      <image:caption>DF2902 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2903</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11156_thumb_P_1465351529670.jpg?v=1592396854</image:loc>
      <image:title>Bcl6 Antibody</image:title>
      <image:caption>DF2903 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2904</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11157_thumb_P_1465351551832.jpg?v=1592396853</image:loc>
      <image:title>beta I Tubulin Antibody</image:title>
      <image:caption>DF2904 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2905</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11158_thumb_P_1465351568666.jpg?v=1592396851</image:loc>
      <image:title>Brd4 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using Brd4 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2906</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11159_thumb_P_1465351584329.jpg?v=1592396849</image:loc>
      <image:title>C10orf63 Antibody</image:title>
      <image:caption>Western blot analysis of C10orf63 using 293 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2907</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11160_thumb_P_1465351600142.jpg?v=1592396848</image:loc>
      <image:title>CaMKII Antibody</image:title>
      <image:caption>DF2907 staining U87 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2908</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11161_thumb_P_1465351615520.jpg?v=1592396846</image:loc>
      <image:title>Caspase-2 Antibody</image:title>
      <image:caption>DF2908 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2909</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11162_thumb_P_1465351633875.jpg?v=1592396844</image:loc>
      <image:title>CCL19 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hybridoma cells, using CCL19 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2910</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11163_thumb_P_1465351654625.jpg?v=1592396843</image:loc>
      <image:title>CCR9 Antibody</image:title>
      <image:caption>DF2910 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2911</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11164_thumb_P_1465351671775.jpg?v=1592396841</image:loc>
      <image:title>CD11b Antibody</image:title>
      <image:caption>DF2911 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2912</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11165_thumb_P_1465351694385.jpg?v=1592396839</image:loc>
      <image:title>CD45 Antibody</image:title>
      <image:caption>DF2912 at 1/100 staining Human pancreas tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2913</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11166_thumb_P_1465351714908.jpg?v=1592396837</image:loc>
      <image:title>Collagen XVII Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using Collagen XVII Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2914</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11167_thumb_P_1465351816113.jpg?v=1592396835</image:loc>
      <image:title>Cubilin Antibody</image:title>
      <image:caption>DF2914 at 1/100 staining Human kidney tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2916</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11168_thumb_P_1465351861548.jpg?v=1592396833</image:loc>
      <image:title>Cytokeratin 19 Antibody</image:title>
      <image:caption>DF2916 staining sw480 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2917</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11169_thumb_P_1465351897421.jpg?v=1592396830</image:loc>
      <image:title>DGCR8 Antibody</image:title>
      <image:caption>DF2917 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2918</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11170_thumb_P_1465351918911.jpg?v=1592396829</image:loc>
      <image:title>DNAJC15 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Myeloma cells, using DNAJC15 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2919</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11171_thumb_P_1465351942064.jpg?v=1592396826</image:loc>
      <image:title>DUSP6 Antibody</image:title>
      <image:caption>DF2919 at 1/100 staining Human gastric tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2920</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11172_thumb_P_1465351957064.jpg?v=1592396824</image:loc>
      <image:title>ENO1 Antibody</image:title>
      <image:caption>DF2920 staining HeLa cells by ICC/IF. Cells were fixed with PFA and permeabilized in 0.1% saponin prior to blocking in 10% serum for 45 minutes at 37¡ãC. The primary antibody was diluted 1/200 and incubated with the sample for 1 hour at 37¡ãC. A  Alexa Fluor 594 conjugated goat polyclonal to rabbit IgG (H+L), diluted 1/600 was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2923</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11173_thumb_P_1465351985598.jpg?v=1592396822</image:loc>
      <image:title>Flotillin 1 Antibody</image:title>
      <image:caption>DF2923 at 1/100 staining Human Melanoma tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2924</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11174_thumb_P_1465352011891.jpg?v=1592396821</image:loc>
      <image:title>FUBP1 Antibody</image:title>
      <image:caption>DF2924 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2925</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11175_thumb_P_1465694589616.jpg?v=1592396819</image:loc>
      <image:title>GATA2/3 Antibody</image:title>
      <image:caption>DF2925 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2926</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11176_thumb_P_1465694623668.jpg?v=1592396817</image:loc>
      <image:title>HAPLN1 Antibody</image:title>
      <image:caption>DF2926 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2927</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11177_thumb_P_1465694655530.jpg?v=1592396815</image:loc>
      <image:title>HDAC11 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using HDAC11 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2928</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11178_thumb_P_1501472101023.jpg?v=1592396814</image:loc>
      <image:title>HIF-2-alpha Antibody</image:title>
      <image:caption>DF2928 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2929</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11179_thumb_P_1465694693723.jpg?v=1592396812</image:loc>
      <image:title>Acetyl-Histone H2A (Lys9) Antibody</image:title>
      <image:caption>DF2929 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2930</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11180_thumb_P_1465694715797.jpg?v=1592396810</image:loc>
      <image:title>Histone H2A.Z Antibody</image:title>
      <image:caption>DF2930 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2931</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11181_thumb_P_1465694753486.jpg?v=1592396809</image:loc>
      <image:title>Histone H3K14me1/2/3 (mono+di+tri methyl K14) Antibody</image:title>
      <image:caption>DF2931 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2932</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df2932_id1_antibody_thumb_P_1548035674601.jpg?v=1592396807</image:loc>
      <image:title>Id1 Antibody</image:title>
      <image:caption>DF2932 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2933</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11183_thumb_P_1465694844289.jpg?v=1592396805</image:loc>
      <image:title>KDEL Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Rat  brain, using KDEL Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2934</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11184_thumb_P_1465694872784.jpg?v=1592396800</image:loc>
      <image:title>KIFC1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using KIFC1 Antibody.
 Lane 1: mouse brain treated with blocking peptide.
 Lane 2: mouse brain;
 Lane 3: hepg2;
 </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2935</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11185_thumb_P_1465695037406.jpg?v=1592396798</image:loc>
      <image:title>LRP1 Antibody</image:title>
      <image:caption>DF2935 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2936</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11186_thumb_P_1465695013680.jpg?v=1592396797</image:loc>
      <image:title>Lrp2 / Megalin Antibody</image:title>
      <image:caption>Western blot analysis of Lrp2 / Megalin using COLO205 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2939</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11187_thumb_P_1465695088591.jpg?v=1592396795</image:loc>
      <image:title>MHC class 1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from VERO, using MHC class 1 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2940</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11188_thumb_P_1465695090373.jpg?v=1592396793</image:loc>
      <image:title>Myb Antibody</image:title>
      <image:caption>DF2940 staining MCF7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2941</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df2941_otx1_antibody_thumb_P_1548035685817.jpg?v=1592396791</image:loc>
      <image:title>Otx1 Antibody</image:title>
      <image:caption>Western blot analysis Otx1 using HepG2 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2942</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11190_thumb_P_1465695244268.jpg?v=1592396790</image:loc>
      <image:title>pan Cadherin Antibody</image:title>
      <image:caption>DF2942 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2943</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11191_thumb_P_1465695221164.jpg?v=1592396788</image:loc>
      <image:title>PD1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using PD1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2944</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11192_thumb_P_1465695272173.jpg?v=1592396787</image:loc>
      <image:title>Phospho-Cdk1/2 (Thr14) Antibody</image:title>
      <image:caption>DF2944 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2945</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11193_thumb_P_1465695308254.jpg?v=1592396785</image:loc>
      <image:title>Phospho-eIF4E (Ser209)  Antibody</image:title>
      <image:caption>DF2945 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2946</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11194_thumb_P_1465695437936.jpg?v=1592396783</image:loc>
      <image:title>Phospho-Histone H1.3 (Thr17) +H1.4 (Thr17) Antibody</image:title>
      <image:caption>DF2946 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2947</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11195_thumb_P_1465695439792.jpg?v=1592396781</image:loc>
      <image:title>Phospho-HSF1 (Ser326) Antibody</image:title>
      <image:caption>DF2947 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2948</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11196_thumb_P_1465695514208.jpg?v=1592396780</image:loc>
      <image:title>Phospho-PAK1/2/3 (Ser144+Ser141+Ser139) Antibody</image:title>
      <image:caption>DF2948 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2949</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11197_thumb_P_1465695523125.jpg?v=1592396778</image:loc>
      <image:title>Phospho-RSK1 p90 (Thr359+Ser363) Antibody</image:title>
      <image:caption>DF2949 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2950</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11198_thumb_P_1465695579911.jpg?v=1592396776</image:loc>
      <image:title>Phospho-Smad5 (Ser463/465) Antibody</image:title>
      <image:caption>DF2950 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2951</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11199_thumb_P_1465695659400.jpg?v=1592396775</image:loc>
      <image:title>PI 3 Kinase p85 beta Antibody</image:title>
      <image:caption>DF2951 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2952</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11200_thumb_P_1465695674669.jpg?v=1592396773</image:loc>
      <image:title>PKC alpha Antibody</image:title>
      <image:caption>DF2952 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2953</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11201_thumb_P_1465695755304.jpg?v=1592396771</image:loc>
      <image:title>PMEL17 / GP100 Antibody</image:title>
      <image:caption>DF2953 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2954</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df2954_ppp1ca_1cb_antibody_thumb_P_1547374480640.jpg?v=1592396769</image:loc>
      <image:title>PPP1CA + 1CB Antibody</image:title>
      <image:caption>DF2954 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2955</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11203_thumb_P_1465695846796.jpg?v=1592396768</image:loc>
      <image:title>PRC1 Antibody</image:title>
      <image:caption>DF2955 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2956</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11204_thumb_P_1465695880587.jpg?v=1592396766</image:loc>
      <image:title>PTBP2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hybridoma cells, using PTBP2 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2957</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11205_thumb_P_1465695888392.jpg?v=1592396764</image:loc>
      <image:title>Rab9 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using Rab9 Antibody.
 Lane 1: Myeloma cells, treated with blocking peptide;
 Lane 2: Myeloma cells;
 Lane 3: Mouse  lung.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2959</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11207_thumb_P_1465695933309.jpg?v=1592396763</image:loc>
      <image:title>Rho A + B + C Antibody</image:title>
      <image:caption>DF2959 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2960</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11208_thumb_P_1465695976373.jpg?v=1592396761</image:loc>
      <image:title>RNF20 Antibody</image:title>
      <image:caption>DF2960 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2962</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11209_thumb_P_1465696045056.jpg?v=1592396759</image:loc>
      <image:title>SATB2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using SATB2 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2963</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11210_thumb_P_1465696062177.jpg?v=1592396758</image:loc>
      <image:title>SNF5 Antibody</image:title>
      <image:caption>Western blot analysis SNF5 using HUVEC whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2964</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11211_thumb_P_1465696087528.jpg?v=1592396756</image:loc>
      <image:title>UCHL3 Antibody</image:title>
      <image:caption>Western blot analysis UCHL3 using HT-29 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2967</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11212_thumb_P_1465696118986.jpg?v=1592396754</image:loc>
      <image:title>YB1 Antibody</image:title>
      <image:caption>DF2967 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2968</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11213_thumb_P_1465696148447.jpg?v=1592396752</image:loc>
      <image:title>TDP43 Antibody</image:title>
      <image:caption>Western blot analysis of TDP43 using HT-29 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2969</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11214_thumb_P_1465696162057.jpg?v=1592396751</image:loc>
      <image:title>Phospho-EGFR ( Tyr1068 ) Antibody</image:title>
      <image:caption>DF2969 staining SK-OV3 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2970</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11215_thumb_P_1465696219145.jpg?v=1592396749</image:loc>
      <image:title>TLR9 Antibody</image:title>
      <image:caption>DF2970 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2971</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11216_thumb_P_1465696255164.jpg?v=1592396747</image:loc>
      <image:title>MSI1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MSI1 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2972</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11217_thumb_P_1465696283656.jpg?v=1592396746</image:loc>
      <image:title>Phospho-DRP1 (Ser616) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-DRP1 (Ser616) using HT-29 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2973</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11218_thumb_P_1465696326194.jpg?v=1592396744</image:loc>
      <image:title>Phospho-EGF Receptor (Tyr998) Antibody</image:title>
      <image:caption>DF2973 staining SK-OV3 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2974</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11219_thumb_P_1465696372325.jpg?v=1592396742</image:loc>
      <image:title>Phospho-EphA2 (Tyr772) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-EphA2 (Tyr772) using HUVEC whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2975</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11220_thumb_P_1465696370806.jpg?v=1592396740</image:loc>
      <image:title>Phospho-PKM2 (Tyr105) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-PKM2 (Tyr105) using K562 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2976</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11221_thumb_P_1465696438284.jpg?v=1592396739</image:loc>
      <image:title>Phospho-RSK2 (Tyr529) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-RSK2 (Tyr529) using HT-29 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2977</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11222_thumb_P_1465696427283.jpg?v=1592396737</image:loc>
      <image:title>Phospho-53BP1 (Ser25/29) Antibody</image:title>
      <image:caption>DF2977 staining COS7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2978</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11223_thumb_P_1465696468035.jpg?v=1592396735</image:loc>
      <image:title>Phospho-53BP1 (Thr543) Antibody</image:title>
      <image:caption>DF2978 staining COS7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2979</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11224_thumb_P_1465696643311.jpg?v=1592396733</image:loc>
      <image:title>Phospho-53BP1 (Ser1778) Antibody</image:title>
      <image:caption>DF2979 staining COS7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2980</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11225_thumb_P_1465696738804.jpg?v=1592396731</image:loc>
      <image:title>Phospho-DRP1 (Ser637) Antibody</image:title>
      <image:caption>DF2980 at 1/100 staining human liver carcinoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2982</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11226_thumb_P_1465696795383.jpg?v=1592396729</image:loc>
      <image:title>Acetyl-alpha-Tubulin (Lys40) Antibody</image:title>
      <image:caption>Western blot analysis of Acetyl-alpha-Tubulin (Lys40) using HeLa whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2983</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11227_thumb_P_1465696836981.jpg?v=1592396727</image:loc>
      <image:title>Phospho-Beclin-1 (Ser93/96) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-Beclin-1 (Ser93/96) using K562 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2984</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11228_thumb_P_1465696997258.jpg?v=1592396725</image:loc>
      <image:title>Phospho-E-Catenin (Ser655/Thr658) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-E-Catenin (Ser655/Thr658) using HUVEC whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2985</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11229_thumb_P_1465697059884.jpg?v=1592396724</image:loc>
      <image:title>Phospho-SQSTM1/p62 (Ser403) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-SQSTM1/p62 (Ser403) using HepG2 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2986</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11230_thumb_P_1465697089552.jpg?v=1592396722</image:loc>
      <image:title>Phospho-SAMHD1 (Thr592) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-SAMHD1 (Thr592) using COLO205 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2987</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11231_thumb_P_1465697122480.jpg?v=1592396720</image:loc>
      <image:title>SAMHD1 Antibody</image:title>
      <image:caption>Western blot analysis SAMHD1 using HepG2 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2988</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11232_thumb_P_1465697147027.jpg?v=1592396718</image:loc>
      <image:title>Phospho-ATR (Ser428) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-ATR (Ser428) using HeLa whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2989</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11233_thumb_P_1465697177650.jpg?v=1592396717</image:loc>
      <image:title>Phospho-Catenin beta (Ser33/37/Thr41) Antibody</image:title>
      <image:caption>DF2989 staining  SW626 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2990</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11234_thumb_P_1465697246300.jpg?v=1592396715</image:loc>
      <image:title>Phospho-PP1 alpha  (Thr320) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-PP1? (Thr320) using HepG2 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2991</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11235_thumb_P_1465697350566.jpg?v=1592396713</image:loc>
      <image:title>PP1 alpha  Antibody</image:title>
      <image:caption>Western blot analysis of PP1? using HeLa whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2992</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11236_thumb_P_1465697463093.jpg?v=1592396708</image:loc>
      <image:title>Phospho-p57 Kip2 (Thr310) Antibody</image:title>
      <image:caption>DF2992 staining K562 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2993</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11237_thumb_P_1465697492445.jpg?v=1592396707</image:loc>
      <image:title>p57 Kip2 Antibody</image:title>
      <image:caption>DF2993 staining K562 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2994</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11238_thumb_P_1465697518329.jpg?v=1592396705</image:loc>
      <image:title>Phospho-LRP6 (Ser1490) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-LRP6 (Ser1490) using HeLa whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2995</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11239_thumb_P_1465697565876.jpg?v=1592396703</image:loc>
      <image:title>LRP6  Antibody</image:title>
      <image:caption>DF2995 at 1/100 staining Mouse colon tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2996</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11240_thumb_P_1465697599476.jpg?v=1592396701</image:loc>
      <image:title>Phospho-FADD (Ser194) Antibody</image:title>
      <image:caption>DF2996 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2997</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11241_thumb_P_1465697658564.jpg?v=1592396700</image:loc>
      <image:title>FADD  Antibody</image:title>
      <image:caption>DF2997 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2998</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11242_thumb_P_1465697806158.jpg?v=1592396698</image:loc>
      <image:title>Phospho-Ack1 (Tyr857/858) Antibody</image:title>
      <image:caption>DF2998 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df2999</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11243_thumb_P_1465697856211.jpg?v=1592396696</image:loc>
      <image:title>Phospho-IP3 Receptor (Ser1756) Antibody</image:title>
      <image:caption>Western blot analysis of Phospho-IP3 Receptor (Ser1756) using HeLa whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3000</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11244_thumb_P_1465698029459.jpg?v=1592396695</image:loc>
      <image:title>IP3 Receptor Antibody</image:title>
      <image:caption>Western blot analysis IP3 Receptor using HUVEC whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3001</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11245_thumb_P_1498268329972.jpg?v=1592396693</image:loc>
      <image:title>JMY Antibody</image:title>
      <image:caption>DF3001 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3002</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11246_thumb_P_1465714252637.jpg?v=1592396691</image:loc>
      <image:title>NKX6.3 Antibody</image:title>
      <image:caption>DF3002 staining K562 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3003</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11247_thumb_P_1465716179254.jpg?v=1592396690</image:loc>
      <image:title>PDLIM1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain and HepG2, using PDLIM1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3004</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11248_thumb_P_1465716238396.jpg?v=1592396688</image:loc>
      <image:title>TAF4 Antibody</image:title>
      <image:caption>DF3004 staining  NIH-3T3 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3005</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11249_thumb_P_1465716277634.jpg?v=1592396686</image:loc>
      <image:title>CDC7 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using CDC7 Antibody.
 Lane 1: Mouse Myeloma cell treated with blocking peptide.
 Lane 2: Mouse Myeloma cell;
 Lane 3: mouse brain;
 </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3006</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11250_thumb_P_1465716344982.jpg?v=1592396685</image:loc>
      <image:title>TTF2 Antibody</image:title>
      <image:caption>DF3006 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3007</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11251_thumb_P_1465716388758.jpg?v=1592396683</image:loc>
      <image:title>VWA5A Antibody</image:title>
      <image:caption>DF3007 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3008</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11252_thumb_P_1465716444059.jpg?v=1592396681</image:loc>
      <image:title>TRIM38 Antibody</image:title>
      <image:caption>DF3008 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3009</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11253_thumb_P_1465716475228.jpg?v=1592396680</image:loc>
      <image:title>TP53I11 Antibody</image:title>
      <image:caption>DF3009 at 1/100 staining Human lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3010</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11254_thumb_P_1465716538464.jpg?v=1592396678</image:loc>
      <image:title>OVOL1 Antibody</image:title>
      <image:caption>DF3010 staining K562 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3011</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11255_thumb_P_1465716592271.jpg?v=1592396676</image:loc>
      <image:title>KNTC2 Antibody</image:title>
      <image:caption>DF3011 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3012</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11256_thumb_P_1465716622913.jpg?v=1592396675</image:loc>
      <image:title>TNFSF11 Antibody</image:title>
      <image:caption>DF3012 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3013</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11257_thumb_P_1465716749369.jpg?v=1592396672</image:loc>
      <image:title>BCKD Antibody</image:title>
      <image:caption>DF3013 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3014</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11258_thumb_P_1465716782266.jpg?v=1592396670</image:loc>
      <image:title>KLF11 Antibody</image:title>
      <image:caption>DF3014 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3015</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11259_thumb_P_1465716842159.jpg?v=1592396668</image:loc>
      <image:title>HGS Antibody</image:title>
      <image:caption>DF3015 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3016</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11260_thumb_P_1465716886217.jpg?v=1592396666</image:loc>
      <image:title>EPHB6 Antibody</image:title>
      <image:caption>DF3016 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3017</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11261_thumb_P_1465716928968.jpg?v=1592396665</image:loc>
      <image:title>TRI18 Antibody</image:title>
      <image:caption>DF3017 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3018</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11262_thumb_P_1465716964178.jpg?v=1592396663</image:loc>
      <image:title>GSC2 Antibody</image:title>
      <image:caption>DF3018 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3019</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11263_thumb_P_1465716997608.jpg?v=1592396661</image:loc>
      <image:title>Clock Antibody</image:title>
      <image:caption>DF3019 staining HUVEC by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3020</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/11264_thumb_P_1465717033055.jpg?v=1592396659</image:loc>
      <image:title>PHF1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using PHF1 Antibody.
 Lane 1: Hybridoma cells, treated with blocking peptide;
 Lane 2: Hybridoma cells;
 Lane 3: Myeloma cells.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3021</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1799_thumb_P_1406633499584.jpg?v=1592396658</image:loc>
      <image:title>ANP32C Antibody</image:title>
      <image:caption>DF3021 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3022</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1800_thumb_P_1406633499240.jpg?v=1592396656</image:loc>
      <image:title>TBX1 Antibody</image:title>
      <image:caption>DF3022 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3023</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1801_thumb_P_1406633499638.jpg?v=1592396654</image:loc>
      <image:title>TNF12 Antibody</image:title>
      <image:caption>DF3023 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3024</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1802_thumb_P_1418191815737.jpg?v=1592396652</image:loc>
      <image:title>AKAP10 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain cells, using AKAP10 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3025</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1803_thumb_P_1418191832517.jpg?v=1592396649</image:loc>
      <image:title>AKAP8 Antibody</image:title>
      <image:caption>DF3025 at 1/100 staining Mouse pancreas tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3026</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1804_thumb_P_1418191855512.jpg?v=1592396647</image:loc>
      <image:title>AIRE Antibody</image:title>
      <image:caption>DF3026 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3027</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1805_thumb_P_1406633499468.jpg?v=1592396645</image:loc>
      <image:title>EFNA2 Antibody</image:title>
      <image:caption>DF3027 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3028</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1806_thumb_P_1406633499500.jpg?v=1592396643</image:loc>
      <image:title>ZNF387 Antibody</image:title>
      <image:caption>DF3028 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3029</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/1807_thumb_P_1406633499978.jpg?v=1592396641</image:loc>
      <image:title>DLX3 Antibody</image:title>
      <image:caption>DF3029 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3031</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2159_thumb_P_1499050909946.jpg?v=1592396639</image:loc>
      <image:title>hnRNP Q Antibody</image:title>
      <image:caption>DF3031 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3032</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2160_thumb_P_1527501282003.jpg?v=1592396637</image:loc>
      <image:title>SDCG1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using SDCG1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3033</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2161_thumb_P_1406633514414.jpg?v=1592396636</image:loc>
      <image:title>BUB1B Antibody</image:title>
      <image:caption>DF3033 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3034</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2185_thumb_P_1406633515969.jpg?v=1592396634</image:loc>
      <image:title>LMX1B Antibody</image:title>
      <image:caption>DF3034 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3035</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2186_thumb_P_1406633515919.jpg?v=1592396632</image:loc>
      <image:title>Musculin Antibody</image:title>
      <image:caption>DF3035 at 1/100 staining Human liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3036</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2187_thumb_P_1418191896126.jpg?v=1592396629</image:loc>
      <image:title>PFKFB2 Antibody</image:title>
      <image:caption>DF3036 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3037</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2188_thumb_P_1418191926590.jpg?v=1592396627</image:loc>
      <image:title>Dyskerin Antibody</image:title>
      <image:caption>DF3037 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3038</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2189_thumb_P_1406633515057.jpg?v=1592396625</image:loc>
      <image:title>PFDN1 Antibody</image:title>
      <image:caption>DF3038 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3039</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2190_thumb_P_1406633515196.jpg?v=1592396623</image:loc>
      <image:title>TBX10 Antibody</image:title>
      <image:caption>DF3039 staining HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3040</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2191_thumb_P_1418191943508.jpg?v=1592396618</image:loc>
      <image:title>TRIM3 Antibody</image:title>
      <image:caption>DF3040 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3041</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2192_thumb_P_1527501260172.jpg?v=1592396615</image:loc>
      <image:title>LAT3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Mouse spleen, using LAT3 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3042</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2193_thumb_P_1418191991812.jpg?v=1592396614</image:loc>
      <image:title>TACC1 Antibody</image:title>
      <image:caption>DF3042 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3043</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2194_thumb_P_1501466403978.jpg?v=1592396612</image:loc>
      <image:title>Maf Antibody</image:title>
      <image:caption>DF3043 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3044</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2195_thumb_P_1406633515419.jpg?v=1592396610</image:loc>
      <image:title>MED24 Antibody</image:title>
      <image:caption>DF3044 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3045</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2196_thumb_P_1504836488787.jpg?v=1592396607</image:loc>
      <image:title>SUPT3H Antibody</image:title>
      <image:caption>DF3045 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3046</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2197_thumb_P_1418192019587.jpg?v=1592396605</image:loc>
      <image:title>TAF5L Antibody</image:title>
      <image:caption>DF3046 staining HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3047</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2198_thumb_P_1525743860811.jpg?v=1592396603</image:loc>
      <image:title>Caper Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using Caper Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3048</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2199_thumb_P_1418192037588.jpg?v=1592396601</image:loc>
      <image:title>BCAR3 Antibody</image:title>
      <image:caption>DF3048 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3049</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2200_thumb_P_1406633515206.jpg?v=1592396599</image:loc>
      <image:title>TALL-2 Antibody</image:title>
      <image:caption>DF3049 at 1/100 staining Mouse colon tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3050</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2201_thumb_P_1406633515936.jpg?v=1592396597</image:loc>
      <image:title>TUSC2 Antibody</image:title>
      <image:caption>DF3050 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3051</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2202_thumb_P_1499952578103.jpg?v=1592396595</image:loc>
      <image:title>DGKI Antibody</image:title>
      <image:caption>DF3051 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3052</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2203_thumb_P_1406633516462.jpg?v=1592396593</image:loc>
      <image:title>ALX3 Antibody</image:title>
      <image:caption>DF3052 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3053</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2204_thumb_P_1406633516340.jpg?v=1592396591</image:loc>
      <image:title>TNFSF15 Antibody</image:title>
      <image:caption>DF3053 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3054</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2205_thumb_P_1406633516773.jpg?v=1592396589</image:loc>
      <image:title>ZNF265 Antibody</image:title>
      <image:caption>DF3054 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3055</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2206_thumb_P_1406633516259.jpg?v=1592396587</image:loc>
      <image:title>LRAT Antibody</image:title>
      <image:caption>DF3055 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3056</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2207_thumb_P_1523768997897.jpg?v=1592396585</image:loc>
      <image:title>MYST2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MYST2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3057</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2208_thumb_P_1523425647974.jpg?v=1592396583</image:loc>
      <image:title>MED26 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MED26 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3058</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2209_thumb_P_1406633516521.jpg?v=1592396581</image:loc>
      <image:title>TNFRSF6B Antibody</image:title>
      <image:caption>DF3058 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3059</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2210_thumb_P_1406633516882.jpg?v=1592396579</image:loc>
      <image:title>SIX6 Antibody</image:title>
      <image:caption>DF3059 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3060</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2211_thumb_P_1406633516822.jpg?v=1592396576</image:loc>
      <image:title>CBX6 Antibody</image:title>
      <image:caption>DF3060 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3061</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2212_thumb_P_1406633516873.jpg?v=1592396574</image:loc>
      <image:title>GAS41 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse lung cells, using GAS41 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3062</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2213_thumb_P_1418192102830.jpg?v=1592396571</image:loc>
      <image:title>ZNF682 Antibody</image:title>
      <image:caption>DF3062 staining COLO205  cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3063</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2214_thumb_P_1499952088068.jpg?v=1592396569</image:loc>
      <image:title>MEKKK 4 Antibody</image:title>
      <image:caption>DF3063 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3064</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2215_thumb_P_1418192122742.jpg?v=1592396567</image:loc>
      <image:title>TOP3B Antibody</image:title>
      <image:caption>DF3064 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3065</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2216_thumb_P_1406633516815.jpg?v=1592396565</image:loc>
      <image:title>PTTG1 Antibody</image:title>
      <image:caption>DF3065 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3066</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2217_thumb_P_1406633516955.jpg?v=1592396563</image:loc>
      <image:title>ACTL6A Antibody</image:title>
      <image:caption>DF3066 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3067</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2218_thumb_P_1406633516156.jpg?v=1592396560</image:loc>
      <image:title>MOS Antibody</image:title>
      <image:caption>DF3067 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3068</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2219_thumb_P_1406633516842.jpg?v=1592396558</image:loc>
      <image:title>ALDOA Antibody</image:title>
      <image:caption>DF3068 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3069</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2220_thumb_P_1406633516424.jpg?v=1592396556</image:loc>
      <image:title>KITH Antibody</image:title>
      <image:caption>DF3069 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3070</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2221_thumb_P_1505976097814.jpg?v=1592396554</image:loc>
      <image:title>HMG17 Antibody</image:title>
      <image:caption>DF3070 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3071</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2222_thumb_P_1406633516040.jpg?v=1592396552</image:loc>
      <image:title>CDC2 Antibody</image:title>
      <image:caption>DF3071 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3072</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2223_thumb_P_1523425665165.jpg?v=1592396550</image:loc>
      <image:title>M-CK Antibody</image:title>
      <image:caption>DF3072 at 1/100 staining Human prostate tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3073</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2224_thumb_P_1498710600281.jpg?v=1592396548</image:loc>
      <image:title>Histone 1F0 Antibody</image:title>
      <image:caption>DF3073 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3074</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2225_thumb_P_1526892873412.jpg?v=1592396546</image:loc>
      <image:title>HEXB Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Rat muscle, using HEXB Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3075</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2226_thumb_P_1406633516922.jpg?v=1592396544</image:loc>
      <image:title>hnRNP C1/C2 Antibody</image:title>
      <image:caption>DF3075 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3076</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2227_thumb_P_1504836517574.jpg?v=1592396541</image:loc>
      <image:title>Adrenergic Receptor  alpha -2A Antibody</image:title>
      <image:caption>DF3076 at 1/100 staining Mouse intestine tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3077</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2228_thumb_P_1406633516349.jpg?v=1592396539</image:loc>
      <image:title>HMGB1 Antibody</image:title>
      <image:caption>DF3077 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3078</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2229_thumb_P_1406633517912.jpg?v=1592396537</image:loc>
      <image:title>HOXC6 Antibody</image:title>
      <image:caption>DF3078 staining  HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3079</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3079_hnrnp_a1_antibody_thumb_P_1548035123021.jpg?v=1592396534</image:loc>
      <image:title>hnRNP A1 Antibody</image:title>
      <image:caption>DF3079 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3080</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3080_tacd2_antibody_thumb_P_1548035123479.jpg?v=1592396533</image:loc>
      <image:title>TACD2 Antibody</image:title>
      <image:caption>DF3080 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3081</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3081_fgr_antibody_thumb_P_1548035123655.jpg?v=1592396527</image:loc>
      <image:title>FGR Antibody</image:title>
      <image:caption>Western blot analysis of extracts of various tissue sample,using FGR Antibody .</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3082</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2233_thumb_P_1406633517894.jpg?v=1592396525</image:loc>
      <image:title>DNA Polymerase  alpha  Antibody</image:title>
      <image:caption>DF3082 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3083</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2234_thumb_P_1505976141555.jpg?v=1592396523</image:loc>
      <image:title>Histone H2AZ Antibody</image:title>
      <image:caption>Western blot analysis of Histone H2AZ expression in various lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3084</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2235_thumb_P_1523425647150.jpg?v=1592396521</image:loc>
      <image:title>HKR1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using HKR1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3085</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2236_thumb_P_1499418347805.jpg?v=1592396519</image:loc>
      <image:title>NR2F6 Antibody</image:title>
      <image:caption>DF3085 at 1/100 staining Mouse pancreas tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3086</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2237_thumb_P_1406633517179.jpg?v=1592396518</image:loc>
      <image:title>TOP2A Antibody</image:title>
      <image:caption>DF3086 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3087</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2238_thumb_P_1523374625121.jpg?v=1592396515</image:loc>
      <image:title>HARS Antibody</image:title>
      <image:caption>DF3087 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3088</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3088_skil_antibody_thumb_P_1548035123560.jpg?v=1592396514</image:loc>
      <image:title>SKIL Antibody</image:title>
      <image:caption>DF3088 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3089</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3089_myf5_antibody_thumb_P_1548035123206.jpg?v=1592396512</image:loc>
      <image:title>MYF5 Antibody</image:title>
      <image:caption>DF3089 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3090</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2241_thumb_P_1406633517287.jpg?v=1592396510</image:loc>
      <image:title>TCTP Antibody</image:title>
      <image:caption>DF3090 at 1/100 staining Rat lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3091</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2242_thumb_P_1523425674281.jpg?v=1592396508</image:loc>
      <image:title>KAP2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using KAP2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3092</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2243_thumb_P_1499953328841.jpg?v=1592396506</image:loc>
      <image:title>GLU2B Antibody</image:title>
      <image:caption>DF3092 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3093</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2244_thumb_P_1530178116010.jpg?v=1592396504</image:loc>
      <image:title>IRF2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using IRF2 Antibody.
 Lane 1: rat brain treated with blocking peptide.
 Lane 2: rat brain;
 Lane 3: mouse brain;
 </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3094</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2162_thumb_P_1418192331813.jpg?v=1592396502</image:loc>
      <image:title>hnRNP L Antibody</image:title>
      <image:caption>DF3094 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3095</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2163_thumb_P_1418192352811.jpg?v=1592396500</image:loc>
      <image:title>B-RAF Antibody</image:title>
      <image:caption>DF3095 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3096</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2164_thumb_P_1406633514954.jpg?v=1592396498</image:loc>
      <image:title>Fra-1 Antibody</image:title>
      <image:caption>DF3096 staining  HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3097</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2165_thumb_P_1529765122185.jpg?v=1592396495</image:loc>
      <image:title>TCF3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using TCF3 Antibody. Lane 1: HepG2  treated with  blocking peptide; Lane 2: HepG2; Lane 3: 293; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3098</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2166_thumb_P_1523425665848.jpg?v=1592396493</image:loc>
      <image:title>PFKFB1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using PFKFB1 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3099</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2167_thumb_P_1406633514343.jpg?v=1592396491</image:loc>
      <image:title>TACD1 Antibody</image:title>
      <image:caption>DF3099 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3100</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2245_thumb_P_1504836544110.jpg?v=1592396489</image:loc>
      <image:title>ZNF18 Antibody</image:title>
      <image:caption>DF3100 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3101</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2246_thumb_P_1504836572617.jpg?v=1592396487</image:loc>
      <image:title>ZNF24 Antibody</image:title>
      <image:caption>DF3101 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3102</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2247_thumb_P_1530178115692.jpg?v=1592396485</image:loc>
      <image:title>UBF1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293,Mouse spleen, using UBF1 Antibody. 
Lane 1: 293 cells treated with the blocking peptide;
Lane 2: 293 cells;
Lane 3: Mouse spleen tissue;</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3103</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2248_thumb_P_1406633517262.jpg?v=1592396483</image:loc>
      <image:title>HOXB9 Antibody</image:title>
      <image:caption>DF3103 staining K562 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3104</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3104_ckmt2_antibody_thumb_P_1548035123757.jpg?v=1592396481</image:loc>
      <image:title>CKMT2 Antibody</image:title>
      <image:caption>DF3104 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3105</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3105_atf7_antibody_thumb_P_1548035123323.jpg?v=1592396479</image:loc>
      <image:title>ATF7 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using ATF7 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3106</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2251_thumb_P_1406633517559.jpg?v=1592396478</image:loc>
      <image:title>KAPC A/B Antibody</image:title>
      <image:caption>DF3106 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3107</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2252_thumb_P_1418192561091.jpg?v=1592396475</image:loc>
      <image:title>K6PL Antibody</image:title>
      <image:caption>DF3107 staining A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3108</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3108_adrenergic_receptor_alpha_2c_antibody_thumb_P_1548035123870.jpg?v=1592396473</image:loc>
      <image:title>Adrenergic Receptor  alpha -2C Antibody</image:title>
      <image:caption>DF3108 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3109</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3109_atf1_antibody_thumb_P_1548035123619.jpg?v=1592396471</image:loc>
      <image:title>ATF1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using ATF1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3110</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2255_thumb_P_1418192618764.jpg?v=1592396469</image:loc>
      <image:title>ATF3 Antibody</image:title>
      <image:caption>DF3110 staining RAW264.7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3111</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2256_thumb_P_1406633518026.jpg?v=1592396467</image:loc>
      <image:title>TSPAN8 Antibody</image:title>
      <image:caption>DF3111 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3112</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2257_thumb_P_1498711074606.jpg?v=1592396465</image:loc>
      <image:title>HXK1 Antibody</image:title>
      <image:caption>DF3112 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3113</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2258_thumb_P_1418192683452.jpg?v=1592396463</image:loc>
      <image:title>TFEB Antibody</image:title>
      <image:caption>DF3113 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3114</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2259_thumb_P_1418192700214.jpg?v=1592396461</image:loc>
      <image:title>TFE3 Antibody</image:title>
      <image:caption>DF3114 at 1/100 staining Mouse colon tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3115</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2260_thumb_P_1406633518310.jpg?v=1592396458</image:loc>
      <image:title>TBP Antibody</image:title>
      <image:caption>DF3115 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3116</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2261_thumb_P_1498268424285.jpg?v=1592396456</image:loc>
      <image:title>TNF Receptor II Antibody</image:title>
      <image:caption>DF3116 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3117</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2262_thumb_P_1406633518979.jpg?v=1592396454</image:loc>
      <image:title>EFNA1 Antibody</image:title>
      <image:caption>DF3117 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3118</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2263_thumb_P_1418192737507.jpg?v=1592396452</image:loc>
      <image:title>CDC2L1 Antibody</image:title>
      <image:caption>DF3118 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3119</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3119_crp1_antibody_thumb_P_1548035122733.jpg?v=1592396450</image:loc>
      <image:title>CRP1 Antibody</image:title>
      <image:caption>DF3119 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3120</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2265_thumb_P_1406633518949.jpg?v=1592396448</image:loc>
      <image:title>EPHA1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from COLO205 cells, using EPHA1 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3121</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2266_thumb_P_1523769006450.jpg?v=1592396446</image:loc>
      <image:title>KAPCG Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat muscle, using KAPCG Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3122</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2267_thumb_P_1498711249604.jpg?v=1592396444</image:loc>
      <image:title>hnRNP A2/B1 Antibody</image:title>
      <image:caption>DF3122 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3123</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3124</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2269_thumb_P_1523769016340.jpg?v=1592396436</image:loc>
      <image:title>S6K Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using S6K Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3125</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2270_thumb_P_1523425648138.jpg?v=1592396434</image:loc>
      <image:title>NFYA Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using NFYA Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3126</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2271_thumb_P_1418192804055.jpg?v=1592396432</image:loc>
      <image:title>IP3KA Antibody</image:title>
      <image:caption>DF3126 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3127</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2272_thumb_P_1523425645093.jpg?v=1592396430</image:loc>
      <image:title>DGKA Antibody</image:title>
      <image:caption>DF3127 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3128</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2273_thumb_P_1406633518394.jpg?v=1592396428</image:loc>
      <image:title>DTYMK Antibody</image:title>
      <image:caption>DF3128 at 1/100 staining Human prostate tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3129</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2274_thumb_P_1523425645488.jpg?v=1592396426</image:loc>
      <image:title>AKAP5 Antibody</image:title>
      <image:caption>DF3129 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3130</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2275_thumb_P_1406633518791.jpg?v=1592396424</image:loc>
      <image:title>CDK2 Antibody</image:title>
      <image:caption>DF3130 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3131</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2276_thumb_P_1406633518575.jpg?v=1592396422</image:loc>
      <image:title>NFYB Antibody</image:title>
      <image:caption>DF3131 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3132</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2277_thumb_P_1406633518485.jpg?v=1592396420</image:loc>
      <image:title>PTX3 Antibody</image:title>
      <image:caption>DF3132 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3133</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2278_thumb_P_1527501278191.jpg?v=1592396417</image:loc>
      <image:title>HMGB2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse lung, using HMGB2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3134</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2279_thumb_P_1406633519767.jpg?v=1592396416</image:loc>
      <image:title>p44 MAPK Antibody</image:title>
      <image:caption>DF3134 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3135</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3135_mark3_antibody_thumb_P_1548035122640.jpg?v=1592396413</image:loc>
      <image:title>MARK3 Antibody</image:title>
      <image:caption>DF3135 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3136</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2281_thumb_P_1508120419070.jpg?v=1592396411</image:loc>
      <image:title>ARNT Antibody</image:title>
      <image:caption>DF3136 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3137</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2282_thumb_P_1406633519384.jpg?v=1592396409</image:loc>
      <image:title>RL10 Antibody</image:title>
      <image:caption>DF3137 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3138</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2283_thumb_P_1406633519763.jpg?v=1592396407</image:loc>
      <image:title>APEX1 Antibody</image:title>
      <image:caption>DF3138 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3139</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2284_thumb_P_1484727196085.jpg?v=1592396405</image:loc>
      <image:title>CALR Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2 and 293, using CALR Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3140</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2285_thumb_P_1504836675658.jpg?v=1592396403</image:loc>
      <image:title>IP3KB Antibody</image:title>
      <image:caption>DF3140 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3141</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2286_thumb_P_1504836747020.jpg?v=1592396401</image:loc>
      <image:title>TEAD1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using TEAD1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3142</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3142_mzf_1_antibody_thumb_P_1548035122024.jpg?v=1592396399</image:loc>
      <image:title>MZF-1 Antibody</image:title>
      <image:caption>DF3142 at 1/100 staining Human lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3143</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2288_thumb_P_1406633519297.jpg?v=1592396397</image:loc>
      <image:title>ERCC5 Antibody</image:title>
      <image:caption>DF3143 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3144</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2289_thumb_P_1406633519773.jpg?v=1592396395</image:loc>
      <image:title>TF2E2 Antibody</image:title>
      <image:caption>DF3144 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3145</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2290_thumb_P_1406633519133.jpg?v=1592396393</image:loc>
      <image:title>EPHA3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293 cells, using EPHA3 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3146</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2291_thumb_P_1498192038766.jpg?v=1592396391</image:loc>
      <image:title>LTK Antibody</image:title>
      <image:caption>DF3146 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3147</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2292_thumb_P_1500020790375.jpg?v=1592396389</image:loc>
      <image:title>PPIF Antibody</image:title>
      <image:caption>DF3147 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3148</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2293_thumb_P_1479369729158.jpg?v=1592396387</image:loc>
      <image:title>CORO1A Antibody</image:title>
      <image:caption>DF3148 at 1/100 staining Human lymph tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3149</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2294_thumb_P_1406633519097.jpg?v=1592396385</image:loc>
      <image:title>HOXA7 Antibody</image:title>
      <image:caption>DF3149 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3150</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2295_thumb_P_1406633519732.jpg?v=1592396383</image:loc>
      <image:title>KAP1 Antibody</image:title>
      <image:caption>DF3150 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3151</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2296_thumb_P_1418192970328.jpg?v=1592396381</image:loc>
      <image:title>GK Antibody</image:title>
      <image:caption>DF3151 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3152</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2297_thumb_P_1505976205849.jpg?v=1592396379</image:loc>
      <image:title>GRK4 Antibody</image:title>
      <image:caption>Western blot analysis GRK4 using HeLa whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3153</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2298_thumb_P_1523425648093.jpg?v=1592396377</image:loc>
      <image:title>FOXN2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from hybridoma cells, using FOXN2 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3154</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2299_thumb_P_1418193020071.jpg?v=1592396375</image:loc>
      <image:title>ELF1 Antibody</image:title>
      <image:caption>DF3154 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3155</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2300_thumb_P_1523425648350.jpg?v=1592396373</image:loc>
      <image:title>TF2H1 Antibody</image:title>
      <image:caption>DF3155 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3156</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2301_thumb_P_1406633519741.jpg?v=1592396371</image:loc>
      <image:title>CD153 Antibody</image:title>
      <image:caption>DF3156 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3157</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2302_thumb_P_1406633519391.jpg?v=1592396369</image:loc>
      <image:title>CIITA Antibody</image:title>
      <image:caption>DF3157 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3158</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2303_thumb_P_1523425648174.jpg?v=1592396367</image:loc>
      <image:title>CSTF2 Antibody</image:title>
      <image:caption>DF3158 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3159</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2304_thumb_P_1523769013270.jpg?v=1592396365</image:loc>
      <image:title>GRK5 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using GRK5 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3160</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2305_thumb_P_1526892873210.jpg?v=1592396363</image:loc>
      <image:title>Recoverin Antibody</image:title>
      <image:caption>DF3160 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3161</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2306_thumb_P_1418193253551.jpg?v=1592396361</image:loc>
      <image:title>RORA Antibody</image:title>
      <image:caption>DF3161 at 1/100 staining Human gastric tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3162</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2307_thumb_P_1406633519486.jpg?v=1592396359</image:loc>
      <image:title>HOXD12 Antibody</image:title>
      <image:caption>DF3162 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3163</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2308_thumb_P_1508462773494.jpg?v=1592396357</image:loc>
      <image:title>Actinin  alpha -2/3 Antibody</image:title>
      <image:caption>DF3163 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3165</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2310_thumb_P_1523425645441.jpg?v=1592396355</image:loc>
      <image:title>GRK3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using GRK3 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3166</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2311_thumb_P_1529920453502.jpg?v=1592396353</image:loc>
      <image:title>ATP7B Antibody</image:title>
      <image:caption>DF3166 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3167</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2312_thumb_P_1523425674231.jpg?v=1592396351</image:loc>
      <image:title>SOX6 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using SOX6 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3168</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2313_thumb_P_1406633520679.jpg?v=1592396345</image:loc>
      <image:title>TCF7 Antibody</image:title>
      <image:caption>DF3168 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3169</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2314_thumb_P_1418193388156.jpg?v=1592396343</image:loc>
      <image:title>ACV1B Antibody</image:title>
      <image:caption>DF3169 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3170</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2315_thumb_P_1418193422393.jpg?v=1592396341</image:loc>
      <image:title>ACVL1 Antibody</image:title>
      <image:caption>DF3170 at 1/100 staining Mouse intestine tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3171</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2316_thumb_P_1406633520007.jpg?v=1592396339</image:loc>
      <image:title>hnRNP G Antibody</image:title>
      <image:caption>DF3171 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3172</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2317_thumb_P_1406633520218.jpg?v=1592396336</image:loc>
      <image:title>FEN1 Antibody</image:title>
      <image:caption>DF3172 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3173</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2318_thumb_P_1406633520832.jpg?v=1592396334</image:loc>
      <image:title>CUTL1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from K562 cells, using CUTL1 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3174</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2319_thumb_P_1418193441808.jpg?v=1592396331</image:loc>
      <image:title>ETV6 Antibody</image:title>
      <image:caption>DF3174 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3175</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2320_thumb_P_1406633520608.jpg?v=1592396329</image:loc>
      <image:title>BUD31 Antibody</image:title>
      <image:caption>DF3175 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3176</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2321_thumb_P_1418193500667.jpg?v=1592396327</image:loc>
      <image:title>CSK Antibody</image:title>
      <image:caption>DF3176 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3177</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2168_thumb_P_1406633514990.jpg?v=1592396325</image:loc>
      <image:title>NBL1 Antibody</image:title>
      <image:caption>DF3177 at 1/100 staining Human lung cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3178</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2169_thumb_P_1406633514525.jpg?v=1592396323</image:loc>
      <image:title>TNFSF9 Antibody</image:title>
      <image:caption>DF3178 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3179</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2170_thumb_P_1418193609733.jpg?v=1592396320</image:loc>
      <image:title>FRK Antibody</image:title>
      <image:caption>DF3179 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3180</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2171_thumb_P_1418193634729.jpg?v=1592396318</image:loc>
      <image:title>GRK6 Antibody</image:title>
      <image:caption>DF3180 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3181</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2172_thumb_P_1505976249888.jpg?v=1592396316</image:loc>
      <image:title>KPB1/2 Antibody</image:title>
      <image:caption>Western blot analysis of Histone KPB1/2 expression in various lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3182</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2173_thumb_P_1418193665454.jpg?v=1592396314</image:loc>
      <image:title>YAP Antibody</image:title>
      <image:caption>DF3182 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3183</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2174_thumb_P_1406633515151.jpg?v=1592396312</image:loc>
      <image:title>ID4 Antibody</image:title>
      <image:caption>DF3183 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3184</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2175_thumb_P_1406633515813.jpg?v=1592396310</image:loc>
      <image:title>TISD Antibody</image:title>
      <image:caption>DF3184 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3185</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2176_thumb_P_1523375015996.jpg?v=1592396308</image:loc>
      <image:title>CKI alpha  Antibody</image:title>
      <image:caption>DF3185 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3186</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2177_thumb_P_1418193703608.jpg?v=1592396306</image:loc>
      <image:title>CDK8 Antibody</image:title>
      <image:caption>DF3186 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3187</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2178_thumb_P_1406633515181.jpg?v=1592396304</image:loc>
      <image:title>HOXA1 Antibody</image:title>
      <image:caption>DF3187 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3188</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2179_thumb_P_1530178116040.jpg?v=1592396302</image:loc>
      <image:title>CKI epsilon Antibody</image:title>
      <image:caption>DF3188 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3189</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2180_thumb_P_1418193730894.jpg?v=1592396300</image:loc>
      <image:title>CLK1 Antibody</image:title>
      <image:caption>DF3189 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3190</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3190_clk2_antibody_thumb_P_1548035122519.jpg?v=1592396298</image:loc>
      <image:title>CLK2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using CLK2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3191</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2182_thumb_P_1406633515146.jpg?v=1592396296</image:loc>
      <image:title>HINT1 Antibody</image:title>
      <image:caption>DF3191 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3192</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2183_thumb_P_1523425674677.jpg?v=1592396294</image:loc>
      <image:title>MEOX2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MEOX2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3193</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2184_thumb_P_1418193808183.jpg?v=1592396292</image:loc>
      <image:title>ER81 Antibody</image:title>
      <image:caption>DF3193 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3194</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2322_thumb_P_1406633520731.jpg?v=1592396290</image:loc>
      <image:title>CD253 Antibody</image:title>
      <image:caption>DF3194 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3195</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2323_thumb_P_1418193839994.jpg?v=1592396288</image:loc>
      <image:title>FXR2 Antibody</image:title>
      <image:caption>DF3195 at 1/100 staining Mouse heart tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3196</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2324_thumb_P_1418193889335.jpg?v=1592396285</image:loc>
      <image:title>RORG Antibody</image:title>
      <image:caption>DF3196 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3197</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2346_thumb_P_1406633521448.jpg?v=1592396283</image:loc>
      <image:title>GALK1 Antibody</image:title>
      <image:caption>DF3197 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3198</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2347_thumb_P_1406633521626.jpg?v=1592396281</image:loc>
      <image:title>BAP31 Antibody</image:title>
      <image:caption>DF3198 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3199</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2348_thumb_P_1418193914575.jpg?v=1592396279</image:loc>
      <image:title>BMX Antibody</image:title>
      <image:caption>DF3199 at 1/100 staining Rat heart tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3200</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2349_thumb_P_1406633521272.jpg?v=1592396277</image:loc>
      <image:title>ZNF75 Antibody</image:title>
      <image:caption>DF3200 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3201</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2350_thumb_P_1418193936645.jpg?v=1592396274</image:loc>
      <image:title>hnRNP M Antibody</image:title>
      <image:caption>DF3201 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3202</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2351_thumb_P_1406633521855.jpg?v=1592396272</image:loc>
      <image:title>NCBP2 Antibody</image:title>
      <image:caption>DF3202 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3203</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2352_thumb_P_1418193960702.jpg?v=1592396270</image:loc>
      <image:title>DGKE Antibody</image:title>
      <image:caption>DF3203 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3204</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2353_thumb_P_1504851531773.jpg?v=1592396267</image:loc>
      <image:title>hnRNP F Antibody</image:title>
      <image:caption>DF3204 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3205</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2354_thumb_P_1406633521418.jpg?v=1592396266</image:loc>
      <image:title>ZNF134 Antibody</image:title>
      <image:caption>DF3205 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3206</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2355_thumb_P_1418193986864.jpg?v=1592396264</image:loc>
      <image:title>RBM5 Antibody</image:title>
      <image:caption>DF3206 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3207</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2356_thumb_P_1406633521212.jpg?v=1592396261</image:loc>
      <image:title>EFNA3 Antibody</image:title>
      <image:caption>DF3207 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3208</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2357_thumb_P_1500636452716.jpg?v=1592396259</image:loc>
      <image:title>EFNA5 Antibody</image:title>
      <image:caption>DF3208 at 1/100 staining Mouse intestine tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3209</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2358_thumb_P_1406633522580.jpg?v=1592396254</image:loc>
      <image:title>DGKQ Antibody</image:title>
      <image:caption>DF3209 staining HT29 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3210</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2359_thumb_P_1406633522452.jpg?v=1592396252</image:loc>
      <image:title>CEBPG Antibody</image:title>
      <image:caption>DF3210 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3211</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2360_thumb_P_1418194044661.jpg?v=1592396250</image:loc>
      <image:title>LIMK2 Antibody</image:title>
      <image:caption>DF3211 at 1/100 staining Mouse pancreas tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3212</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2361_thumb_P_1504851559776.jpg?v=1592396248</image:loc>
      <image:title>MAPK10 Antibody</image:title>
      <image:caption>DF3212 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3213</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2362_thumb_P_1406633522112.jpg?v=1592396246</image:loc>
      <image:title>PTTG Antibody</image:title>
      <image:caption>DF3213 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3214</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2363_thumb_P_1523769006222.jpg?v=1592396244</image:loc>
      <image:title>PRKAG1/2/3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using PRKAG1/2/3 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3215</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2364_thumb_P_1406633522654.jpg?v=1592396242</image:loc>
      <image:title>EPHB4 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293 cells using EPHB4 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3216</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2365_thumb_P_1406633522647.jpg?v=1592396239</image:loc>
      <image:title>AF10 Antibody</image:title>
      <image:caption>DF3216 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3217</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2366_thumb_P_1418194064136.jpg?v=1592396237</image:loc>
      <image:title>ELL Antibody</image:title>
      <image:caption>DF3217 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3218</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2367_thumb_P_1406633522048.jpg?v=1592396235</image:loc>
      <image:title>ADK Antibody</image:title>
      <image:caption>DF3218 staining  RAW264.7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3219</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2368_thumb_P_1504851588592.jpg?v=1592396233</image:loc>
      <image:title>hnRNP H Antibody</image:title>
      <image:caption>DF3219 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3220</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2369_thumb_P_1406633522836.jpg?v=1592396231</image:loc>
      <image:title>DLX5 Antibody</image:title>
      <image:caption>DF3220 at 1/100 staining Mouse heart tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3221</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2370_thumb_P_1418194093164.jpg?v=1592396229</image:loc>
      <image:title>CKS1 Antibody</image:title>
      <image:caption>DF3221 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3222</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2371_thumb_P_1418194115695.jpg?v=1592396227</image:loc>
      <image:title>COPS2 Antibody</image:title>
      <image:caption>DF3222 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3223</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2372_thumb_P_1406633522473.jpg?v=1592396225</image:loc>
      <image:title>LMO4 Antibody</image:title>
      <image:caption>DF3223 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3224</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2373_thumb_P_1406633522021.jpg?v=1592396223</image:loc>
      <image:title>PITX1 Antibody</image:title>
      <image:caption>DF3224 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3225</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2374_thumb_P_1406633522387.jpg?v=1592396220</image:loc>
      <image:title>IRX1 Antibody</image:title>
      <image:caption>DF3225 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3226</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2375_thumb_P_1406633522598.jpg?v=1592396218</image:loc>
      <image:title>ST5 Antibody</image:title>
      <image:caption>DF3226 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3227</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2376_thumb_P_1523768997848.jpg?v=1592396216</image:loc>
      <image:title>ADARB1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using ADARB1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3228</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2377_thumb_P_1406633522998.jpg?v=1592396214</image:loc>
      <image:title>SSBP2 Antibody</image:title>
      <image:caption>DF3228 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3229</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2378_thumb_P_1529920453075.jpg?v=1592396212</image:loc>
      <image:title>CRBP III Antibody</image:title>
      <image:caption>DF3229 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3230</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2379_thumb_P_1406633522157.jpg?v=1592396210</image:loc>
      <image:title>SFRS3 Antibody</image:title>
      <image:caption>DF3230 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3231</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2380_thumb_P_1418194159402.jpg?v=1592396208</image:loc>
      <image:title>FOXK1 Antibody</image:title>
      <image:caption>DF3231 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3232</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2381_thumb_P_1529920453465.jpg?v=1592396206</image:loc>
      <image:title>TFAM Antibody</image:title>
      <image:caption>DF3232 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3233</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2382_thumb_P_1406633523406.jpg?v=1592396204</image:loc>
      <image:title>CDKL1 Antibody</image:title>
      <image:caption>DF3233 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3234</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2383_thumb_P_1523769006283.jpg?v=1592396202</image:loc>
      <image:title>K6PP Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using K6PP Antibody. Lane 1: mouse brain  treated with  blocking peptide; Lane 2: mouse brain; Lane 3: rat brain; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3235</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2384_thumb_P_1504851651828.jpg?v=1592396200</image:loc>
      <image:title>SFRS17A Antibody</image:title>
      <image:caption>DF3235 staining  NIH-3T3 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3236</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2385_thumb_P_1406633523726.jpg?v=1592396198</image:loc>
      <image:title>MEF2B Antibody</image:title>
      <image:caption>DF3236 staining HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3237</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2386_thumb_P_1406633523169.jpg?v=1592396196</image:loc>
      <image:title>CREM Antibody</image:title>
      <image:caption>DF3237 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3238</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2387_thumb_P_1406633523480.jpg?v=1592396194</image:loc>
      <image:title>Mevalonate Kinase Antibody</image:title>
      <image:caption>DF3238 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3239</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2388_thumb_P_1406633523795.jpg?v=1592396192</image:loc>
      <image:title>TLE2 Antibody</image:title>
      <image:caption>DF3239 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3240</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2389_thumb_P_1527501296424.jpg?v=1592396190</image:loc>
      <image:title>MtSSB Antibody</image:title>
      <image:caption>Western blot analysis of extracts from MCF7, using MtSSB Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3241</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2390_thumb_P_1504851693203.jpg?v=1592396188</image:loc>
      <image:title>CSTF1 Antibody</image:title>
      <image:caption>DF3241 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3242</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2391_thumb_P_1406633523349.jpg?v=1592396186</image:loc>
      <image:title>SRY Antibody</image:title>
      <image:caption>DF3242 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3243</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2392_thumb_P_1500020876043.jpg?v=1592396184</image:loc>
      <image:title>TNFC Antibody</image:title>
      <image:caption>DF3243 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3244</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2393_thumb_P_1525743861473.jpg?v=1592396182</image:loc>
      <image:title>TNFRSF9 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, rat heart, using TNFRSF9 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3245</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2394_thumb_P_1418194216446.jpg?v=1592396180</image:loc>
      <image:title>SFRS4 Antibody</image:title>
      <image:caption>DF3245 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3246</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2395_thumb_P_1418194243414.jpg?v=1592396178</image:loc>
      <image:title>NCBP1 Antibody</image:title>
      <image:caption>DF3246 staining  HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3247</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2396_thumb_P_1406633523410.jpg?v=1592396176</image:loc>
      <image:title>MN1 Antibody</image:title>
      <image:caption>DF3247 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3248</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2397_thumb_P_1523425675560.jpg?v=1592396174</image:loc>
      <image:title>TEF Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat heart, using TEF Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3249</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2398_thumb_P_1491360128638.jpg?v=1592396173</image:loc>
      <image:title>AKAP13 Antibody</image:title>
      <image:caption>DF3249 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3250</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2399_thumb_P_1523425675565.jpg?v=1592396171</image:loc>
      <image:title>Nuclear Factor 1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using Nuclear Factor 1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3251</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2400_thumb_P_1523425675499.jpg?v=1592396169</image:loc>
      <image:title>ELAVL2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using ELAVL2 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3252</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2401_thumb_P_1523768998825.jpg?v=1592396164</image:loc>
      <image:title>FOXC1/2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HUVEC, using FOXC1/2 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3253</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2402_thumb_P_1406633524881.jpg?v=1592396162</image:loc>
      <image:title>FOXL1 Antibody</image:title>
      <image:caption>DF3253 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3254</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2403_thumb_P_1498711327068.jpg?v=1592396160</image:loc>
      <image:title>CAF1A Antibody</image:title>
      <image:caption>Western blot analysis of CAF1A  expression in mouse brain lysate</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3255</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2404_thumb_P_1523425675339.jpg?v=1592396158</image:loc>
      <image:title>CAF1B Antibody</image:title>
      <image:caption>DF3255 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3256</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2405_thumb_P_1406633524204.jpg?v=1592396156</image:loc>
      <image:title>PSMD2 Antibody</image:title>
      <image:caption>DF3256 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3257</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2406_thumb_P_1418194419614.jpg?v=1592396154</image:loc>
      <image:title>CGK 2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HUVEC cells, using CGK 2 antibody.The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3258</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2325_thumb_P_1523375015947.jpg?v=1592396151</image:loc>
      <image:title>MTA1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using MTA1 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3259</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2326_thumb_P_1500020956863.jpg?v=1592396149</image:loc>
      <image:title>KLF Antibody</image:title>
      <image:caption>DF3259 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3260</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2327_thumb_P_1529777200889.jpg?v=1592396148</image:loc>
      <image:title>JIP2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using JIP2 Antibody. Lane 1: HepG2  treated with  antigen-specific peptide; Lane 2: HepG2; Lane 3: hela; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3261</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2328_thumb_P_1530178116837.jpg?v=1592396145</image:loc>
      <image:title>TCOF1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using TCOF1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3262</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2329_thumb_P_1406633520081.jpg?v=1592396144</image:loc>
      <image:title>TUSC3 Antibody</image:title>
      <image:caption>DF3262 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3263</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2330_thumb_P_1406633520142.jpg?v=1592396142</image:loc>
      <image:title>FOXE3 Antibody</image:title>
      <image:caption>DF3263 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3264</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2331_thumb_P_1406633520672.jpg?v=1592396139</image:loc>
      <image:title>Myelodysplasia Syndrome 1 Antibody</image:title>
      <image:caption>DF3264 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3265</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2332_thumb_P_1406633520750.jpg?v=1592396137</image:loc>
      <image:title>TOP3A Antibody</image:title>
      <image:caption>DF3265 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3266</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2333_thumb_P_1418194487625.jpg?v=1592396135</image:loc>
      <image:title>Smad4 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HeLa cells using Smad4 antibody.The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3267</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2334_thumb_P_1406633520493.jpg?v=1592396133</image:loc>
      <image:title>TDG Antibody</image:title>
      <image:caption>DF3267 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3268</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2335_thumb_P_1504851722687.jpg?v=1592396131</image:loc>
      <image:title>ITPK1 Antibody</image:title>
      <image:caption>DF3268 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3269</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2336_thumb_P_1406633520133.jpg?v=1592396129</image:loc>
      <image:title>TRA-2 alpha  Antibody</image:title>
      <image:caption>DF3269 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3270</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2407_thumb_P_1500021026503.jpg?v=1592396127</image:loc>
      <image:title>DYR1A Antibody</image:title>
      <image:caption>DF3270 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3271</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2408_thumb_P_1406633524819.jpg?v=1592396125</image:loc>
      <image:title>TNAP1 Antibody</image:title>
      <image:caption>DF3271 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3272</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2409_thumb_P_1418194521236.jpg?v=1592396123</image:loc>
      <image:title>TF2H2 Antibody</image:title>
      <image:caption>DF3272 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3273</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2410_thumb_P_1530178115031.jpg?v=1592396121</image:loc>
      <image:title>CBF beta Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using CBF ? Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3274</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2411_thumb_P_1499427167676.jpg?v=1592396119</image:loc>
      <image:title>GIT2 Antibody</image:title>
      <image:caption>DF3274 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3275</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2412_thumb_P_1504851856226.jpg?v=1592396117</image:loc>
      <image:title>E2F2 Antibody</image:title>
      <image:caption>DF3275 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3276</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2413_thumb_P_1418194552504.jpg?v=1592396115</image:loc>
      <image:title>ZNF147 Antibody</image:title>
      <image:caption>DF3276 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3277</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2414_thumb_P_1418194569561.jpg?v=1592396113</image:loc>
      <image:title>Glucokinase Regulator Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse heart cells using Glucokinase Regulator antibody,The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3278</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2415_thumb_P_1418194590822.jpg?v=1592396110</image:loc>
      <image:title>MELK Antibody</image:title>
      <image:caption>DF3278 staining K562 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3279</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2416_thumb_P_1499427242805.jpg?v=1592396108</image:loc>
      <image:title>HLX1 Antibody</image:title>
      <image:caption>DF3279 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3280</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2417_thumb_P_1406633524168.jpg?v=1592396106</image:loc>
      <image:title>ZNF638 Antibody</image:title>
      <image:caption>DF3280 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3281</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2418_thumb_P_1418194623940.jpg?v=1592396104</image:loc>
      <image:title>FAKD3 Antibody</image:title>
      <image:caption>DF3281 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3282</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2419_thumb_P_1523425675654.jpg?v=1592396102</image:loc>
      <image:title>WTAP Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using WTAP Antibody. Lane 1: mouse brain  treated with  blocking peptide; Lane 2: mouse brain; Lane 3: rat brain; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3283</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2420_thumb_P_1406633524295.jpg?v=1592396100</image:loc>
      <image:title>PSMD2 Antibody</image:title>
      <image:caption>DF3283 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3284</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2421_thumb_P_1406633524188.jpg?v=1592396098</image:loc>
      <image:title>CDK5R1 Antibody</image:title>
      <image:caption>DF3284 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3285</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2422_thumb_P_1406633524424.jpg?v=1592396096</image:loc>
      <image:title>CDK10 Antibody</image:title>
      <image:caption>DF3285 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3286</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2423_thumb_P_1505976289503.jpg?v=1592396094</image:loc>
      <image:title>PDGFRL Antibody</image:title>
      <image:caption>Western blot analysis of Histone PDGFRL expression in various lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3287</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2424_thumb_P_1406633524091.jpg?v=1592396092</image:loc>
      <image:title>ANKRD1 Antibody</image:title>
      <image:caption>DF3287 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3288</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2425_thumb_P_1406633525765.jpg?v=1592396090</image:loc>
      <image:title>EPHA7 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Jurkat cells using EPHA7 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3289</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2426_thumb_P_1501466527598.jpg?v=1592396087</image:loc>
      <image:title>SURF1 Antibody</image:title>
      <image:caption>DF3289 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3290</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2427_thumb_P_1418194643471.jpg?v=1592396085</image:loc>
      <image:title>TAF5 Antibody</image:title>
      <image:caption>DF3290 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3291</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2428_thumb_P_1418194658290.jpg?v=1592396082</image:loc>
      <image:title>TAF1A Antibody</image:title>
      <image:caption>DF3291 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3292</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2429_thumb_P_1406633525980.jpg?v=1592396080</image:loc>
      <image:title>TSN Antibody</image:title>
      <image:caption>DF3292 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3293</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2430_thumb_P_1498267993169.jpg?v=1592396073</image:loc>
      <image:title>TRIP13 Antibody</image:title>
      <image:caption>DF3293 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3294</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2431_thumb_P_1498711418430.jpg?v=1592396071</image:loc>
      <image:title>MED1 Antibody</image:title>
      <image:caption>DF3294 at 1/100 staining Mouse colon tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3295</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2432_thumb_P_1418194688801.jpg?v=1592396069</image:loc>
      <image:title>TRIP4 Antibody</image:title>
      <image:caption>DF3295 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3296</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2433_thumb_P_1406633525116.jpg?v=1592396067</image:loc>
      <image:title>RhoH Antibody</image:title>
      <image:caption>DF3296 staining HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3297</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2434_thumb_P_1406633525471.jpg?v=1592396065</image:loc>
      <image:title>TSC22D1 Antibody</image:title>
      <image:caption>DF3297 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3298</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2435_thumb_P_1418195083148.jpg?v=1592396062</image:loc>
      <image:title>NAB2 Antibody</image:title>
      <image:caption>DF3298 at 1/100 staining Human gastric tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3299</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2436_thumb_P_1406633525589.jpg?v=1592396060</image:loc>
      <image:title>CEBPE Antibody</image:title>
      <image:caption>DF3299 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3300</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2437_thumb_P_1418195113789.jpg?v=1592396058</image:loc>
      <image:title>Smad1/5/9 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HeLa cells, using Smad1/5/9 antibody.The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3301</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2438_thumb_P_1500636373961.jpg?v=1592396056</image:loc>
      <image:title>VPS72 Antibody</image:title>
      <image:caption>DF3301 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3302</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2439_thumb_P_1406633525498.jpg?v=1592396054</image:loc>
      <image:title>MAPK3 Antibody</image:title>
      <image:caption>DF3302 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3303</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2440_thumb_P_1504851886810.jpg?v=1592396052</image:loc>
      <image:title>NFIL3 Antibody</image:title>
      <image:caption>DF3303 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3304</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2441_thumb_P_1418195162806.jpg?v=1592396050</image:loc>
      <image:title>p97 MAPK Antibody</image:title>
      <image:caption>DF3304 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3305</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2442_thumb_P_1418195186146.jpg?v=1592396048</image:loc>
      <image:title>ZNF187 Antibody</image:title>
      <image:caption>DF3305 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3306</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2443_thumb_P_1500021200819.jpg?v=1592396046</image:loc>
      <image:title>DGKD Antibody</image:title>
      <image:caption>DF3306 staining  HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3307</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2444_thumb_P_1418195206080.jpg?v=1592396043</image:loc>
      <image:title>PFKFB3 Antibody</image:title>
      <image:caption>DF3307 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3308</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2445_thumb_P_1418195332658.jpg?v=1592396041</image:loc>
      <image:title>DOK7 Antibody</image:title>
      <image:caption>DF3308 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3309</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2446_thumb_P_1523425644513.jpg?v=1592396039</image:loc>
      <image:title>AAK1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using AAK1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3310</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2447_thumb_P_1418195382398.jpg?v=1592396037</image:loc>
      <image:title>DAK Antibody</image:title>
      <image:caption>DF3310 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3311</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2448_thumb_P_1526892873103.jpg?v=1592396034</image:loc>
      <image:title>ADCK5 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse lung , using ADCK5 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3312</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2449_thumb_P_1418195436898.jpg?v=1592396033</image:loc>
      <image:title>CERKL Antibody</image:title>
      <image:caption>DF3312 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3313</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2450_thumb_P_1504851921849.jpg?v=1592396031</image:loc>
      <image:title>PLCH Antibody</image:title>
      <image:caption>DF3313 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3314</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2451_thumb_P_1504851952075.jpg?v=1592396029</image:loc>
      <image:title>TSSC1 Antibody</image:title>
      <image:caption>DF3314 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3315</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2452_thumb_P_1418195461831.jpg?v=1592396027</image:loc>
      <image:title>FAKD1 Antibody</image:title>
      <image:caption>DF3315 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3316</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2453_thumb_P_1418195477647.jpg?v=1592396025</image:loc>
      <image:title>SGOL1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HeLa cells, using SGOL1 antibody.The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3317</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2454_thumb_P_1406633525167.jpg?v=1592396022</image:loc>
      <image:title>CDKL4 Antibody</image:title>
      <image:caption>DF3317 at 1/100 staining Human gastric tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3319</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2456_thumb_P_1498710925810.jpg?v=1592396020</image:loc>
      <image:title>RBM26 Antibody</image:title>
      <image:caption>DF3319 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3320</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2457_thumb_P_1504851979805.jpg?v=1592396018</image:loc>
      <image:title>TTC23 Antibody</image:title>
      <image:caption>DF3320 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3321</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2458_thumb_P_1418195516074.jpg?v=1592396016</image:loc>
      <image:title>STEA3 Antibody</image:title>
      <image:caption>DF3321 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3322</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2459_thumb_P_1529765091917.jpg?v=1592396014</image:loc>
      <image:title>STEAP4 Antibody</image:title>
      <image:caption>DF3322 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3323</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2460_thumb_P_1406633526278.jpg?v=1592396012</image:loc>
      <image:title>LDOC1L Antibody</image:title>
      <image:caption>DF3323 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3324</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2461_thumb_P_1498625294175.jpg?v=1592396010</image:loc>
      <image:title>MAST2 Antibody</image:title>
      <image:caption>DF3324 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3325</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2462_thumb_P_1406633526701.jpg?v=1592396009</image:loc>
      <image:title>SFXN4 Antibody</image:title>
      <image:caption>DF3325 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3326</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2463_thumb_P_1406633526522.jpg?v=1592396006</image:loc>
      <image:title>TNFAIP8L2 Antibody</image:title>
      <image:caption>DF3326 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3327</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2464_thumb_P_1406633526390.jpg?v=1592396004</image:loc>
      <image:title>DOK6 Antibody</image:title>
      <image:caption>DF3327 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3328</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2465_thumb_P_1406633526104.jpg?v=1592396002</image:loc>
      <image:title>KSR2 Antibody</image:title>
      <image:caption>DF3328 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3329</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3329_mark2_antibody_thumb_P_1548035122678.jpg?v=1592396000</image:loc>
      <image:title>MARK2 Antibody</image:title>
      <image:caption>DF3329 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3330</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2467_thumb_P_1418196329447.jpg?v=1592395998</image:loc>
      <image:title>ARMCX2 Antibody</image:title>
      <image:caption>DF3330 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3331</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2468_thumb_P_1418196387792.jpg?v=1592395995</image:loc>
      <image:title>DOK3 Antibody</image:title>
      <image:caption>DF3331 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3332</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2469_thumb_P_1406633526502.jpg?v=1592395993</image:loc>
      <image:title>MAEA Antibody</image:title>
      <image:caption>DF3332 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3333</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2470_thumb_P_1406633526091.jpg?v=1592395991</image:loc>
      <image:title>MOL1A Antibody</image:title>
      <image:caption>DF3333 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3334</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2471_thumb_P_1406633526386.jpg?v=1592395989</image:loc>
      <image:title>STRAD Antibody</image:title>
      <image:caption>DF3334 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3335</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2472_thumb_P_1418196419765.jpg?v=1592395987</image:loc>
      <image:title>ADCK2 Antibody</image:title>
      <image:caption>DF3335 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3336</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2473_thumb_P_1406633526769.jpg?v=1592395982</image:loc>
      <image:title>ATPBD3 Antibody</image:title>
      <image:caption>DF3336 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3337</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2474_thumb_P_1406633526414.jpg?v=1592395979</image:loc>
      <image:title>MOBKL2B Antibody</image:title>
      <image:caption>DF3337 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3338</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2475_thumb_P_1418196450231.jpg?v=1592395977</image:loc>
      <image:title>ADCK1 Antibody</image:title>
      <image:caption>DF3338 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3339</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2476_thumb_P_1406633526012.jpg?v=1592395975</image:loc>
      <image:title>MAGI2 Antibody</image:title>
      <image:caption>DF3339 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3340</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2477_thumb_P_1406633526486.jpg?v=1592395972</image:loc>
      <image:title>AKAP14 Antibody</image:title>
      <image:caption>DF3340 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3341</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2478_thumb_P_1406633526636.jpg?v=1592395970</image:loc>
      <image:title>SIAH Antibody</image:title>
      <image:caption>DF3341 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3342</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2479_thumb_P_1406633526856.jpg?v=1592395968</image:loc>
      <image:title>MAP4K3 Antibody</image:title>
      <image:caption>DF3342 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3343</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2480_thumb_P_1500021296174.jpg?v=1592395966</image:loc>
      <image:title>TRIM59 Antibody</image:title>
      <image:caption>DF3343 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3344</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2481_thumb_P_1523425667683.jpg?v=1592395964</image:loc>
      <image:title>LMTK2 Antibody</image:title>
      <image:caption>DF3344 at 1/100 staining Human brain cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3345</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2482_thumb_P_1500021363290.jpg?v=1592395962</image:loc>
      <image:title>TUSC5 Antibody</image:title>
      <image:caption>DF3345 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3346</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2483_thumb_P_1418196471245.jpg?v=1592395960</image:loc>
      <image:title>TBC1D3 Antibody</image:title>
      <image:caption>DF3346 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3347</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2484_thumb_P_1406633526475.jpg?v=1592395958</image:loc>
      <image:title>FUK Antibody</image:title>
      <image:caption>DF3347 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3348</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2485_thumb_P_1406633527968.jpg?v=1592395956</image:loc>
      <image:title>KIAA1967 Antibody</image:title>
      <image:caption>DF3348 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3349</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2486_thumb_P_1500021406634.jpg?v=1592395954</image:loc>
      <image:title>DCLK2 Antibody</image:title>
      <image:caption>DF3349 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3350</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2487_thumb_P_1501466714632.jpg?v=1592395952</image:loc>
      <image:title>SPIC Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using SPIC Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3351</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2488_thumb_P_1418196567622.jpg?v=1592395950</image:loc>
      <image:title>CAMK5 Antibody</image:title>
      <image:caption>DF3351 at 1/100 staining Mouse intestine tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3352</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2337_thumb_P_1418196630831.jpg?v=1592395948</image:loc>
      <image:title>HIPK4 Antibody</image:title>
      <image:caption>DF3352 at 1/100 staining Rat brain tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3353</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2338_thumb_P_1418196689479.jpg?v=1592395946</image:loc>
      <image:title>ACRBP Antibody</image:title>
      <image:caption>DF3353 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3354</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2339_thumb_P_1406633520685.jpg?v=1592395944</image:loc>
      <image:title>RGAG1 Antibody</image:title>
      <image:caption>DF3354 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3355</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2340_thumb_P_1418196745245.jpg?v=1592395942</image:loc>
      <image:title>PPHLN Antibody</image:title>
      <image:caption>DF3355 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3356</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2341_thumb_P_1418196790804.jpg?v=1592395939</image:loc>
      <image:title>ZNF397 Antibody</image:title>
      <image:caption>DF3356 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3357</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2342_thumb_P_1418196812782.jpg?v=1592395937</image:loc>
      <image:title>ANKK1 Antibody</image:title>
      <image:caption>DF3357 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3358</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2343_thumb_P_1523769013518.jpg?v=1592395935</image:loc>
      <image:title>BAF250B Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using BAF250B Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3359</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2344_thumb_P_1406633521763.jpg?v=1592395933</image:loc>
      <image:title>IPMK Antibody</image:title>
      <image:caption>DF3359 staining HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3360</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2345_thumb_P_1504852007127.jpg?v=1592395931</image:loc>
      <image:title>ADCK3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using ADCK3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3361</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2489_thumb_P_1526892873455.jpg?v=1592395930</image:loc>
      <image:title>PPP1R14C Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using PPP1R14C Antibody. Lane 1: 293  treated with  blocking peptide; Lane 2: 293; Lane 3: mouse brain; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3362</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2490_thumb_P_1406633527437.jpg?v=1592395928</image:loc>
      <image:title>LMO3 Antibody</image:title>
      <image:caption>DF3362 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3363</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2491_thumb_P_1406633527084.jpg?v=1592395926</image:loc>
      <image:title>SMRC2 Antibody</image:title>
      <image:caption>DF3363 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3364</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2516_thumb_P_1406634050844.jpg?v=1592395923</image:loc>
      <image:title>RIN3 Antibody</image:title>
      <image:caption>DF3364 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3365</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2517_thumb_P_1418196836005.jpg?v=1592395921</image:loc>
      <image:title>ZNF596 Antibody</image:title>
      <image:caption>DF3365 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3366</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2518_thumb_P_1418196852543.jpg?v=1592395919</image:loc>
      <image:title>BRSK1 Antibody</image:title>
      <image:caption>DF3366 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3367</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2519_thumb_P_1418196882255.jpg?v=1592395917</image:loc>
      <image:title>ES8L1 Antibody</image:title>
      <image:caption>DF3367 at 1/100 staining Human urothelial cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3368</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2520_thumb_P_1500021473118.jpg?v=1592395914</image:loc>
      <image:title>PARD3 Antibody</image:title>
      <image:caption>DF3368 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3369</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2521_thumb_P_1501466774835.jpg?v=1592395913</image:loc>
      <image:title>DOK4 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse muscle, using DOK4 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3370</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2522_thumb_P_1418196938653.jpg?v=1592395911</image:loc>
      <image:title>GRK7 Antibody</image:title>
      <image:caption>DF3370 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3371</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2523_thumb_P_1406634050397.jpg?v=1592395909</image:loc>
      <image:title>DUSP19 Antibody</image:title>
      <image:caption>DF3371 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3372</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2524_thumb_P_1523425648484.jpg?v=1592395906</image:loc>
      <image:title>GTF3C2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using GTF3C2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3373</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2525_thumb_P_1406634050940.jpg?v=1592395904</image:loc>
      <image:title>ORAOV1 Antibody</image:title>
      <image:caption>DF3373 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3374</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2526_thumb_P_1406634050044.jpg?v=1592395902</image:loc>
      <image:title>MADD Antibody</image:title>
      <image:caption>DF3374 at 1/100 staining Human brain cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3375</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2527_thumb_P_1406634050038.jpg?v=1592395900</image:loc>
      <image:title>CNKR2 Antibody</image:title>
      <image:caption>DF3375 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3376</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2528_thumb_P_1406634050972.jpg?v=1592395898</image:loc>
      <image:title>BRI3B Antibody</image:title>
      <image:caption>DF3376 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3377</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2529_thumb_P_1406634050744.jpg?v=1592395896</image:loc>
      <image:title>SMG7 Antibody</image:title>
      <image:caption>DF3377 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3378</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2530_thumb_P_1418197035921.jpg?v=1592395890</image:loc>
      <image:title>AKAP1 Antibody</image:title>
      <image:caption>DF3378 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3379</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2531_thumb_P_1523769004629.jpg?v=1592395888</image:loc>
      <image:title>CDKL2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using CDKL2 Antibody.
 Lane 1: rat brain treated with blocking peptide.
 Lane 2: rat brain;
 Lane 3: mouse spleen;
 </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3380</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2532_thumb_P_1406634050485.jpg?v=1592395886</image:loc>
      <image:title>REQU Antibody</image:title>
      <image:caption>DF3380 staining HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3381</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2533_thumb_P_1418197082958.jpg?v=1592395884</image:loc>
      <image:title>EZH1 Antibody</image:title>
      <image:caption>DF3381 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3382</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2534_thumb_P_1530178115221.jpg?v=1592395882</image:loc>
      <image:title>TAF15 Antibody</image:title>
      <image:caption>DF3382 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3383</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2535_thumb_P_1500021531585.jpg?v=1592395879</image:loc>
      <image:title>GCN5L2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain cells, using GCN5L2 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3384</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2536_thumb_P_1418197164448.jpg?v=1592395878</image:loc>
      <image:title>CELF-1 Antibody</image:title>
      <image:caption>DF3384 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3385</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2537_thumb_P_1500021590943.jpg?v=1592395876</image:loc>
      <image:title>MEKKK 1 Antibody</image:title>
      <image:caption>DF3385 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3386</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2538_thumb_P_1418197212934.jpg?v=1592395874</image:loc>
      <image:title>FOXJ1 Antibody</image:title>
      <image:caption>DF3386 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3387</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2539_thumb_P_1406634051311.jpg?v=1592395872</image:loc>
      <image:title>DLX4 Antibody</image:title>
      <image:caption>DF3387 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3388</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2540_thumb_P_1418197229336.jpg?v=1592395869</image:loc>
      <image:title>BRF1 Antibody</image:title>
      <image:caption>DF3388 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3389</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2541_thumb_P_1418197255834.jpg?v=1592395867</image:loc>
      <image:title>CNKSR1 Antibody</image:title>
      <image:caption>DF3389 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3390</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2542_thumb_P_1418197277175.jpg?v=1592395865</image:loc>
      <image:title>MKL1 Antibody</image:title>
      <image:caption>DF3390 staining  HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3391</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2543_thumb_P_1406634051821.jpg?v=1592395863</image:loc>
      <image:title>PMEPA1 Antibody</image:title>
      <image:caption>DF3391 at 1/100 staining Human prostate tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3392</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2544_thumb_P_1406634051010.jpg?v=1592395861</image:loc>
      <image:title>ISL2 Antibody</image:title>
      <image:caption>DF3392 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3393</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2545_thumb_P_1418197308224.jpg?v=1592395859</image:loc>
      <image:title>JAKMIP2 Antibody</image:title>
      <image:caption>DF3393 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3394</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2546_thumb_P_1505178741891.jpg?v=1592395857</image:loc>
      <image:title>ORCTL-2 Antibody</image:title>
      <image:caption>DF3394 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3395</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2547_thumb_P_1406634051666.jpg?v=1592395855</image:loc>
      <image:title>MOBKL2A/B Antibody</image:title>
      <image:caption>DF3395 staining NIH-3T3 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3396</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2548_thumb_P_1406634051135.jpg?v=1592395853</image:loc>
      <image:title>RASD2 Antibody</image:title>
      <image:caption>DF3396 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3397</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2549_thumb_P_1406634051839.jpg?v=1592395851</image:loc>
      <image:title>IP3KC Antibody</image:title>
      <image:caption>DF3397 staining  HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3398</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2550_thumb_P_1523769004531.jpg?v=1592395849</image:loc>
      <image:title>MASTL Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MASTL Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3399</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2551_thumb_P_1418197343236.jpg?v=1592395847</image:loc>
      <image:title>PGBD1 Antibody</image:title>
      <image:caption>DF3399 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3400</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2552_thumb_P_1418197362923.jpg?v=1592395845</image:loc>
      <image:title>ZNF668 Antibody</image:title>
      <image:caption>DF3400 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3401</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2553_thumb_P_1406634051731.jpg?v=1592395843</image:loc>
      <image:title>FAM84B Antibody</image:title>
      <image:caption>DF3401 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3402</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2554_thumb_P_1418197391328.jpg?v=1592395840</image:loc>
      <image:title>PKNOX2 Antibody</image:title>
      <image:caption>DF3402 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3403</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2555_thumb_P_1505178771901.jpg?v=1592395838</image:loc>
      <image:title>IP6K3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse muscle, using IP6K3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3404</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2556_thumb_P_1406634051588.jpg?v=1592395836</image:loc>
      <image:title>LMTK3 Antibody</image:title>
      <image:caption>DF3404 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3405</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2557_thumb_P_1406634051931.jpg?v=1592395834</image:loc>
      <image:title>AL2S7 Antibody</image:title>
      <image:caption>DF3405 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3406</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2558_thumb_P_1406634051147.jpg?v=1592395832</image:loc>
      <image:title>CIB3 Antibody</image:title>
      <image:caption>DF3406 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3407</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2559_thumb_P_1406634051076.jpg?v=1592395830</image:loc>
      <image:title>ALPK1 Antibody</image:title>
      <image:caption>DF3407 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3408</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2560_thumb_P_1406634051300.jpg?v=1592395828</image:loc>
      <image:title>RPS6KC1 Antibody</image:title>
      <image:caption>DF3408 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3409</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2561_thumb_P_1418197844180.jpg?v=1592395826</image:loc>
      <image:title>SERINC2 Antibody</image:title>
      <image:caption>DF3409 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3410</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2562_thumb_P_1418197870795.jpg?v=1592395824</image:loc>
      <image:title>MAP3K3 Antibody</image:title>
      <image:caption>DF3410 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3411</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2563_thumb_P_1406634051987.jpg?v=1592395822</image:loc>
      <image:title>FOXB1/2 Antibody</image:title>
      <image:caption>DF3411 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3412</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2564_thumb_P_1527501277314.jpg?v=1592395819</image:loc>
      <image:title>ATF6B Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using ATF6B Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3413</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2565_thumb_P_1500637565048.jpg?v=1592395818</image:loc>
      <image:title>DUSP9 Antibody</image:title>
      <image:caption>DF3413 at 1/100 staining Rat heart tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3414</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2566_thumb_P_1406634051394.jpg?v=1592395816</image:loc>
      <image:title>ADPGK Antibody</image:title>
      <image:caption>DF3414 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3415</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2567_thumb_P_1418197909575.jpg?v=1592395814</image:loc>
      <image:title>TINF2 Antibody</image:title>
      <image:caption>DF3415 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3416</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2568_thumb_P_1406634051235.jpg?v=1592395812</image:loc>
      <image:title>MMTAG2 Antibody</image:title>
      <image:caption>DF3416 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3417</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2569_thumb_P_1505178810731.jpg?v=1592395810</image:loc>
      <image:title>MKNK1 Antibody</image:title>
      <image:caption>DF3417 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3418</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2570_thumb_P_1418197933417.jpg?v=1592395808</image:loc>
      <image:title>UTP14A Antibody</image:title>
      <image:caption>DF3418 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3419</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2571_thumb_P_1418197960787.jpg?v=1592395806</image:loc>
      <image:title>NADAP Antibody</image:title>
      <image:caption>DF3419 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3420</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2572_thumb_P_1406634052090.jpg?v=1592395800</image:loc>
      <image:title>NARG1 Antibody</image:title>
      <image:caption>DF3420 staining  HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3421</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2573_thumb_P_1406634052669.jpg?v=1592395798</image:loc>
      <image:title>AN30A Antibody</image:title>
      <image:caption>DF3421 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3422</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2492_thumb_P_1418198013927.jpg?v=1592395796</image:loc>
      <image:title>YTHDF1 Antibody</image:title>
      <image:caption>DF3422 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3423</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2493_thumb_P_1523769006766.jpg?v=1592395793</image:loc>
      <image:title>IFIH1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using IFIH1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3424</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2494_thumb_P_1504852040722.jpg?v=1592395792</image:loc>
      <image:title>ZNF436 Antibody</image:title>
      <image:caption>DF3424 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3425</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2495_thumb_P_1504852076671.jpg?v=1592395790</image:loc>
      <image:title>BHLHB3 Antibody</image:title>
      <image:caption>DF3425 staining RAW264.7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3426</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2496_thumb_P_1406633527125.jpg?v=1592395788</image:loc>
      <image:title>PBOV1 Antibody</image:title>
      <image:caption>DF3426 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3427</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2497_thumb_P_1499418141426.jpg?v=1592395785</image:loc>
      <image:title>ILKAP Antibody</image:title>
      <image:caption>DF3427 at 1/100 staining Human liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3428</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2498_thumb_P_1418198061484.jpg?v=1592395783</image:loc>
      <image:title>ZNF541 Antibody</image:title>
      <image:caption>DF3428 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3429</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2499_thumb_P_1406633527058.jpg?v=1592395781</image:loc>
      <image:title>XRN2 Antibody</image:title>
      <image:caption>DF3429 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3430</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2500_thumb_P_1406633527572.jpg?v=1592395778</image:loc>
      <image:title>NT5C3 Antibody</image:title>
      <image:caption>DF3430 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3431</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2501_thumb_P_1523769012101.jpg?v=1592395776</image:loc>
      <image:title>SLK Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat lung, using SLK Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3432</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2502_thumb_P_1406633527722.jpg?v=1592395775</image:loc>
      <image:title>BLZF1 Antibody</image:title>
      <image:caption>DF3432 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3433</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2503_thumb_P_1504852117897.jpg?v=1592395773</image:loc>
      <image:title>MUC13 Antibody</image:title>
      <image:caption>DF3433 at 1/100 staining Mouse kidney tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3434</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2504_thumb_P_1418198082187.jpg?v=1592395771</image:loc>
      <image:title>SEMA4A Antibody</image:title>
      <image:caption>DF3434 at 1/100 staining Mouse intestine tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3435</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2505_thumb_P_1406633527968.jpg?v=1592395768</image:loc>
      <image:title>PRDM12 Antibody</image:title>
      <image:caption>DF3435 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3436</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2506_thumb_P_1406633527051.jpg?v=1592395766</image:loc>
      <image:title>ZNF435 Antibody</image:title>
      <image:caption>DF3436 staining NIH-3T3 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3437</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2507_thumb_P_1504852223053.jpg?v=1592395764</image:loc>
      <image:title>AZI2 Antibody</image:title>
      <image:caption>DF3437 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3438</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2574_thumb_P_1505178843089.jpg?v=1592395762</image:loc>
      <image:title>FKRP Antibody</image:title>
      <image:caption>DF3438 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3439</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2575_thumb_P_1406634052787.jpg?v=1592395760</image:loc>
      <image:title>LASS4 Antibody</image:title>
      <image:caption>DF3439 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3440</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2576_thumb_P_1418198104417.jpg?v=1592395758</image:loc>
      <image:title>ZNF287 Antibody</image:title>
      <image:caption>DF3440 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3441</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2577_thumb_P_1418198152259.jpg?v=1592395756</image:loc>
      <image:title>ARNT2 Antibody</image:title>
      <image:caption>DF3441 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3442</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2578_thumb_P_1527501282031.jpg?v=1592395754</image:loc>
      <image:title>BRMS1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using BRMS1 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3443</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2579_thumb_P_1418198169028.jpg?v=1592395753</image:loc>
      <image:title>DCP1A Antibody</image:title>
      <image:caption>DF3443 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3444</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2580_thumb_P_1527501282233.jpg?v=1592395749</image:loc>
      <image:title>BCA3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat lung, using BCA3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3445</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2581_thumb_P_1406634052537.jpg?v=1592395747</image:loc>
      <image:title>DUSP22 Antibody</image:title>
      <image:caption>DF3445 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3446</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2582_thumb_P_1505178877355.jpg?v=1592395745</image:loc>
      <image:title>SERC1 Antibody</image:title>
      <image:caption>DF3446 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3447</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2583_thumb_P_1406634052417.jpg?v=1592395743</image:loc>
      <image:title>CREBZF Antibody</image:title>
      <image:caption>DF3447 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3448</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2584_thumb_P_1523374625459.jpg?v=1592395741</image:loc>
      <image:title>IARS2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2,mouse brain, using IARS2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3449</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2585_thumb_P_1418198187588.jpg?v=1592395739</image:loc>
      <image:title>MED17 Antibody</image:title>
      <image:caption>DF3449 staining HT29 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3450</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2586_thumb_P_1406634052762.jpg?v=1592395737</image:loc>
      <image:title>EKI2 Antibody</image:title>
      <image:caption>DF3450 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3451</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2587_thumb_P_1406634052696.jpg?v=1592395735</image:loc>
      <image:title>DNAJC17 Antibody</image:title>
      <image:caption>DF3451 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3452</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2588_thumb_P_1418198218759.jpg?v=1592395733</image:loc>
      <image:title>DUS2L Antibody</image:title>
      <image:caption>DF3452 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3453</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2589_thumb_P_1527501334404.jpg?v=1592395731</image:loc>
      <image:title>AATF Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using AATF Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3454</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2590_thumb_P_1418198265734.jpg?v=1592395729</image:loc>
      <image:title>MLTK Antibody</image:title>
      <image:caption>DF3454 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3456</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2592_thumb_P_1406634052958.jpg?v=1592395727</image:loc>
      <image:title>E2AK3 Antibody</image:title>
      <image:caption>DF3456 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3457</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2593_thumb_P_1508462548999.jpg?v=1592395725</image:loc>
      <image:title>MARK Antibody</image:title>
      <image:caption>Western blot analysis of MARK expression in various lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3458</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2594_thumb_P_1406634052842.jpg?v=1592395723</image:loc>
      <image:title>HMG20B Antibody</image:title>
      <image:caption>DF3458 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3459</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2595_thumb_P_1418198371716.jpg?v=1592395720</image:loc>
      <image:title>DNMT3B Antibody</image:title>
      <image:caption>DF3459 at 1/100 staining Mouse spleen tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3460</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2596_thumb_P_1406634052767.jpg?v=1592395718</image:loc>
      <image:title>LW-1 Antibody</image:title>
      <image:caption>DF3460 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3462</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2598_thumb_P_1418198422064.jpg?v=1592395716</image:loc>
      <image:title>DBF4 Antibody</image:title>
      <image:caption>DF3462 staining NIH-3T3 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3463</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2599_thumb_P_1406634052974.jpg?v=1592395709</image:loc>
      <image:title>MORF4L1 Antibody</image:title>
      <image:caption>DF3463 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3464</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2600_thumb_P_1529777201493.jpg?v=1592395706</image:loc>
      <image:title>EPHA6 Antibody</image:title>
      <image:caption>DF3464 staining U87 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3465</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2601_thumb_P_1527501283092.jpg?v=1592395704</image:loc>
      <image:title>ZC3H7B Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using ZC3H7B Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3466</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2602_thumb_P_1500637643197.jpg?v=1592395703</image:loc>
      <image:title>Mlx Antibody</image:title>
      <image:caption>DF3466 staining  LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3467</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2603_thumb_P_1529765091730.jpg?v=1592395701</image:loc>
      <image:title>TRPS1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using TRPS1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3468</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2604_thumb_P_1418198473291.jpg?v=1592395699</image:loc>
      <image:title>CARKL Antibody</image:title>
      <image:caption>DF3468 at 1/100 staining Human brain cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3469</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2605_thumb_P_1406634052469.jpg?v=1592395696</image:loc>
      <image:title>CNOT7 Antibody</image:title>
      <image:caption>DF3469 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3470</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2606_thumb_P_1406634052348.jpg?v=1592395694</image:loc>
      <image:title>STAG3 Antibody</image:title>
      <image:caption>DF3470 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3471</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2607_thumb_P_1505178908942.jpg?v=1592395691</image:loc>
      <image:title>FOXD3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using FOXD3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3472</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2608_thumb_P_1418198489805.jpg?v=1592395689</image:loc>
      <image:title>IKZF3 Antibody</image:title>
      <image:caption>DF3472 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3473</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2609_thumb_P_1406634053519.jpg?v=1592395687</image:loc>
      <image:title>JIP3 Antibody</image:title>
      <image:caption>DF3473 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3475</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2611_thumb_P_1418198520228.jpg?v=1592395685</image:loc>
      <image:title>CDK11 Antibody</image:title>
      <image:caption>DF3475 staining COLO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3476</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2612_thumb_P_1418198537071.jpg?v=1592395683</image:loc>
      <image:title>ZNF148 Antibody</image:title>
      <image:caption>DF3476 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3477</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2613_thumb_P_1406634053448.jpg?v=1592395681</image:loc>
      <image:title>CHKB Antibody</image:title>
      <image:caption>DF3477 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3478</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2614_thumb_P_1406634053599.jpg?v=1592395679</image:loc>
      <image:title>ERGI3 Antibody</image:title>
      <image:caption>DF3478 staining  LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3479</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2615_thumb_P_1406634053099.jpg?v=1592395677</image:loc>
      <image:title>ASF1A Antibody</image:title>
      <image:caption>DF3479 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3480</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2616_thumb_P_1406634053010.jpg?v=1592395675</image:loc>
      <image:title>ATF5 Antibody</image:title>
      <image:caption>DF3480 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3481</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2617_thumb_P_1418198584478.jpg?v=1592395673</image:loc>
      <image:title>AKAP2 Antibody</image:title>
      <image:caption>DF3481 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3482</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2618_thumb_P_1406634053181.jpg?v=1592395671</image:loc>
      <image:title>YBOX2 Antibody</image:title>
      <image:caption>DF3482 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3483</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2619_thumb_P_1498625147543.jpg?v=1592395669</image:loc>
      <image:title>TBX22 Antibody</image:title>
      <image:caption>DF3483 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3484</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2620_thumb_P_1527501283971.jpg?v=1592395667</image:loc>
      <image:title>DYR1B Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using DYR1B Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3486</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2622_thumb_P_1406634054943.jpg?v=1592395665</image:loc>
      <image:title>SUPT16H Antibody</image:title>
      <image:caption>DF3486 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3487</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2623_thumb_P_1418198661560.jpg?v=1592395663</image:loc>
      <image:title>IRAK1 Antibody</image:title>
      <image:caption>DF3487 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3488</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2624_thumb_P_1406634054259.jpg?v=1592395661</image:loc>
      <image:title>SPIN1 Antibody</image:title>
      <image:caption>DF3488 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3489</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2625_thumb_P_1527501298635.jpg?v=1592395659</image:loc>
      <image:title>EID1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using EID1 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3490</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2626_thumb_P_1406634054470.jpg?v=1592395657</image:loc>
      <image:title>14-3-3 beta Antibody</image:title>
      <image:caption>DF3490 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3491</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2627_thumb_P_1527501306255.jpg?v=1592395655</image:loc>
      <image:title>14-3-3 epsilon Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293 and rat brain mouse lung, using 14-3-3 ? Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3492</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2628_thumb_P_1406634054061.jpg?v=1592395652</image:loc>
      <image:title>14-3-3 eta Antibody</image:title>
      <image:caption>DF3492 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3493</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2629_thumb_P_1523375501108.jpg?v=1592395650</image:loc>
      <image:title>14-3-3 gamma Antibody</image:title>
      <image:caption>DF3493 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3494</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2630_thumb_P_1406634054590.jpg?v=1592395648</image:loc>
      <image:title>14-3-3 theta Antibody</image:title>
      <image:caption>DF3494 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3495</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2631_thumb_P_1508462668218.jpg?v=1592395646</image:loc>
      <image:title>14-3-3 zeta/delta Antibody</image:title>
      <image:caption>DF3495 staining  NIH-3T3 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3496</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2632_thumb_P_1406634054196.jpg?v=1592395643</image:loc>
      <image:title>5-HT-1A Antibody</image:title>
      <image:caption>DF3496 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3497</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2633_thumb_P_1505178976666.jpg?v=1592395641</image:loc>
      <image:title>5-HT-1B Antibody</image:title>
      <image:caption>DF3497 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3498</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2634_thumb_P_1406634054151.jpg?v=1592395639</image:loc>
      <image:title>5-HT-1E Antibody</image:title>
      <image:caption>DF3498 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3499</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2635_thumb_P_1501466851221.jpg?v=1592395637</image:loc>
      <image:title>5-HT-1F Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela,HepG2,rat brain, using 5-HT-1F Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3500</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2636_thumb_P_1527501261333.jpg?v=1592395636</image:loc>
      <image:title>5-HT-2B Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using 5-HT-2B Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3501</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2637_thumb_P_1418198704020.jpg?v=1592395634</image:loc>
      <image:title>5-HT-2C Antibody</image:title>
      <image:caption>DF3501 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3502</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2638_thumb_P_1418198736976.jpg?v=1592395632</image:loc>
      <image:title>5-HT-3A Antibody</image:title>
      <image:caption>DF3502 staining HT29 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3503</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2639_thumb_P_1406634054627.jpg?v=1592395630</image:loc>
      <image:title>5-HT-4 Antibody</image:title>
      <image:caption>DF3503 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3504</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2640_thumb_P_1406634054778.jpg?v=1592395628</image:loc>
      <image:title>5-HT-5A Antibody</image:title>
      <image:caption>DF3504 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3505</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2641_thumb_P_1406634054653.jpg?v=1592395626</image:loc>
      <image:title>5-HT-6 Antibody</image:title>
      <image:caption>DF3505 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3506</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2642_thumb_P_1501466921814.jpg?v=1592395623</image:loc>
      <image:title>ADRA1A Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using ADRA1A Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3507</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2643_thumb_P_1406634054141.jpg?v=1592395618</image:loc>
      <image:title>ADCY4 Antibody</image:title>
      <image:caption>DF3507 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3508</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2644_thumb_P_1406634054276.jpg?v=1592395616</image:loc>
      <image:title>ADCY5/6 Antibody</image:title>
      <image:caption>DF3508 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3509</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2645_thumb_P_1418198753664.jpg?v=1592395614</image:loc>
      <image:title>ADD2 Antibody</image:title>
      <image:caption>DF3509 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3510</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2646_thumb_P_1498711628762.jpg?v=1592395612</image:loc>
      <image:title>ADD3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using ADD3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3511</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2647_thumb_P_1505179006223.jpg?v=1592395610</image:loc>
      <image:title>ADRB1 Antibody</image:title>
      <image:caption>DF3511 staining  HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3512</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2648_thumb_P_1418198801127.jpg?v=1592395608</image:loc>
      <image:title>ADRB2 Antibody</image:title>
      <image:caption>DF3512 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3513</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2649_thumb_P_1406634054621.jpg?v=1592395606</image:loc>
      <image:title>AHSA1 Antibody</image:title>
      <image:caption>DF3513 staining HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3514</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2650_thumb_P_1523769016498.jpg?v=1592395603</image:loc>
      <image:title>AIM2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using AIM2 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3515</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2651_thumb_P_1418198845957.jpg?v=1592395602</image:loc>
      <image:title>API-5 Antibody</image:title>
      <image:caption>DF3515 at 1/100 staining Mouse pancreas tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3516</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2652_thumb_P_1505179035757.jpg?v=1592395600</image:loc>
      <image:title>ARRB1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using ARRB1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3517</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2653_thumb_P_1523769011704.jpg?v=1592395598</image:loc>
      <image:title>ARRDC3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293 and mouse brain, using ARRDC3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3518</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2508_thumb_P_1406634050737.jpg?v=1592395596</image:loc>
      <image:title>AS250 Antibody</image:title>
      <image:caption>DF3518 at 1/100 staining Mouse kidney tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3519</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2509_thumb_P_1418198863163.jpg?v=1592395594</image:loc>
      <image:title>AVEN Antibody</image:title>
      <image:caption>DF3519 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3520</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2510_thumb_P_1527501298642.jpg?v=1592395592</image:loc>
      <image:title>BCOR Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using BCOR Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3521</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2511_thumb_P_1406634050858.jpg?v=1592395590</image:loc>
      <image:title>BUB3 Antibody</image:title>
      <image:caption>DF3521 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3522</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2512_thumb_P_1406634050976.jpg?v=1592395588</image:loc>
      <image:title>CD160 Antibody</image:title>
      <image:caption>DF3522 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3523</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2513_thumb_P_1495802402084.jpg?v=1592395586</image:loc>
      <image:title>CDH11 Antibody</image:title>
      <image:caption>DF3523 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3524</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2514_thumb_P_1525743861673.jpg?v=1592395584</image:loc>
      <image:title>CDH15 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using CDH15 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3525</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2515_thumb_P_1418200195128.jpg?v=1592395582</image:loc>
      <image:title>CDH16 Antibody</image:title>
      <image:caption>DF3525 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3526</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2654_thumb_P_1527501299284.jpg?v=1592395580</image:loc>
      <image:title>CDH17 Antibody</image:title>
      <image:caption>DF3526 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3527</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2655_thumb_P_1527501261133.jpg?v=1592395578</image:loc>
      <image:title>CDH18 Antibody</image:title>
      <image:caption>DF3527 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3528</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2656_thumb_P_1418200249013.jpg?v=1592395576</image:loc>
      <image:title>CDH19 Antibody</image:title>
      <image:caption>DF3528 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3529</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2657_thumb_P_1418200277290.jpg?v=1592395574</image:loc>
      <image:title>CDH22 Antibody</image:title>
      <image:caption>DF3529 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3530</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2658_thumb_P_1406634055466.jpg?v=1592395572</image:loc>
      <image:title>CDH2 Antibody</image:title>
      <image:caption>DF3530 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3531</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2659_thumb_P_1527501261181.jpg?v=1592395570</image:loc>
      <image:title>CDH3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using CDH3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3532</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2660_thumb_P_1418200327671.jpg?v=1592395568</image:loc>
      <image:title>CDH7 Antibody</image:title>
      <image:caption>DF3532 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3533</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2661_thumb_P_1418200359561.jpg?v=1592395566</image:loc>
      <image:title>CDH8 Antibody</image:title>
      <image:caption>DF3533 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3534</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2662_thumb_P_1501467039581.jpg?v=1592395564</image:loc>
      <image:title>CDH9 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using CDH9 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3535</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2663_thumb_P_1505976394840.jpg?v=1592395561</image:loc>
      <image:title>CADM1 Antibody</image:title>
      <image:caption>DF3535 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3536</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2683_thumb_P_1501467108600.jpg?v=1592395559</image:loc>
      <image:title>CADM2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2,mouse brain, using CADM2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3537</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2684_thumb_P_1527501261019.jpg?v=1592395556</image:loc>
      <image:title>CADM3 Antibody</image:title>
      <image:caption>DF3537 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3538</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2685_thumb_P_1501467163584.jpg?v=1592395554</image:loc>
      <image:title>CADM4 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using CADM4 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3539</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2686_thumb_P_1406634056869.jpg?v=1592395552</image:loc>
      <image:title>TMEM30B Antibody</image:title>
      <image:caption>DF3539 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3540</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2687_thumb_P_1525743861242.jpg?v=1592395549</image:loc>
      <image:title>Cytochrome c-type Heme Lyase Antibody</image:title>
      <image:caption>DF3540 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3541</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2688_thumb_P_1523769011821.jpg?v=1592395548</image:loc>
      <image:title>CCRL1 Antibody</image:title>
      <image:caption>DF3541 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3542</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2689_thumb_P_1505179060477.jpg?v=1592395546</image:loc>
      <image:title>p55CDC Antibody</image:title>
      <image:caption>DF3542 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3543</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2690_thumb_P_1501467237551.jpg?v=1592395543</image:loc>
      <image:title>CDCA2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using CDCA2 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3544</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2691_thumb_P_1406634056987.jpg?v=1592395541</image:loc>
      <image:title>CDCA3 Antibody</image:title>
      <image:caption>DF3544 at 1/100 staining Human prostate tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3545</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2692_thumb_P_1523769006490.jpg?v=1592395539</image:loc>
      <image:title>CDCA7 Antibody</image:title>
      <image:caption>DF3545 staining Hela by IF/ICC. The samples were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. Samples were then incubated with primary Ab(DF3545 1:200) and mouse anti-beta tubulin Ab(T0023 1:200) for 1 hour at 37¡ãC. An  AlexaFluor594 conjugated goat anti-rabbit IgG(H+L) Ab(S0006 Red 1:600) and an AlexaFluor488 conjugated goat anti-mouse IgG(H+L) Ab(S0017 Green 1:600) were used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3546</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2693_thumb_P_1501467318517.jpg?v=1592395537</image:loc>
      <image:title>CDKAL Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using CDKAL Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3547</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2694_thumb_P_1418200428347.jpg?v=1592395536</image:loc>
      <image:title>CDK5RAP3 Antibody</image:title>
      <image:caption>DF3547 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3548</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2695_thumb_P_1527501287169.jpg?v=1592395533</image:loc>
      <image:title>CMKLR1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse brain, using CMKLR1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3549</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2696_thumb_P_1501467396867.jpg?v=1592395528</image:loc>
      <image:title>Collagen I  alpha 2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using Collagen I ?2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3550</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2697_thumb_P_1523425668106.jpg?v=1592395526</image:loc>
      <image:title>Collagen IV  alpha 2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using Collagen IV ?2 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3551</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2698_thumb_P_1523425668302.jpg?v=1592395524</image:loc>
      <image:title>Collagen V  alpha 1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using Collagen V ?1 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3552</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2699_thumb_P_1501467461776.jpg?v=1592395522</image:loc>
      <image:title>Collagen VI  alpha 2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using Collagen VI ?2 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3553</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2700_thumb_P_1406634056855.jpg?v=1592395520</image:loc>
      <image:title>Collagen XI  alpha 1 Antibody</image:title>
      <image:caption>DF3553 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3554</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2701_thumb_P_1418200466116.jpg?v=1592395517</image:loc>
      <image:title>Collagen XIII  alpha 1 Antibody</image:title>
      <image:caption>DF3554 staining NIH-3T3 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3555</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2702_thumb_P_1406634056611.jpg?v=1592395515</image:loc>
      <image:title>Collagen XX  alpha 1 Antibody</image:title>
      <image:caption>DF3555 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3556</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2703_thumb_P_1418200488685.jpg?v=1592395513</image:loc>
      <image:title>Collagen XXV  alpha 1 Antibody</image:title>
      <image:caption>DF3556 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3557</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2704_thumb_P_1406634056398.jpg?v=1592395511</image:loc>
      <image:title>COX11 Antibody</image:title>
      <image:caption>DF3557 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3558</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2705_thumb_P_1418200509034.jpg?v=1592395508</image:loc>
      <image:title>COX17 Antibody</image:title>
      <image:caption>DF3558 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3560</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2707_thumb_P_1406634056017.jpg?v=1592395506</image:loc>
      <image:title>COX42 Antibody</image:title>
      <image:caption>DF3560 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3561</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2708_thumb_P_1505179150246.jpg?v=1592395504</image:loc>
      <image:title>COX5A Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using COX5A Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3562</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2709_thumb_P_1501467543926.jpg?v=1592395502</image:loc>
      <image:title>COX6C Antibody</image:title>
      <image:caption>DF3562 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3563</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2710_thumb_P_1505179186273.jpg?v=1592395500</image:loc>
      <image:title>Cytochrome P450 17A1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293 and Hela, using Cytochrome P450 17A1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3564</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2711_thumb_P_1499427397818.jpg?v=1592395498</image:loc>
      <image:title>Cytochrome P450 19A1 Antibody</image:title>
      <image:caption>DF3564 at 1/100 staining Human brain cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3565</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2712_thumb_P_1418200537703.jpg?v=1592395496</image:loc>
      <image:title>Cytochrome P450 1A1/2 Antibody</image:title>
      <image:caption>DF3565 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3566</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2713_thumb_P_1501467812473.jpg?v=1592395494</image:loc>
      <image:title>Cytochrome P450 1A2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Myeloma cells, using Cytochrome P450 1A2 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3567</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2714_thumb_P_1418200554310.jpg?v=1592395492</image:loc>
      <image:title>Cytochrome P450 21A2 Antibody</image:title>
      <image:caption>DF3567 staining 293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3568</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2715_thumb_P_1418200613922.jpg?v=1592395490</image:loc>
      <image:title>Cytochrome P450 24A1 Antibody</image:title>
      <image:caption>DF3568 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3569</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2716_thumb_P_1418200633586.jpg?v=1592395488</image:loc>
      <image:title>Cytochrome P450 26A1 Antibody</image:title>
      <image:caption>DF3569 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3570</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2717_thumb_P_1529920346123.jpg?v=1592395486</image:loc>
      <image:title>Cytochrome P450 26C1 Antibody</image:title>
      <image:caption>DF3570 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3571</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2718_thumb_P_1418200652200.jpg?v=1592395484</image:loc>
      <image:title>Cytochrome P450 27A1 Antibody</image:title>
      <image:caption>DF3571 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3572</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2719_thumb_P_1418200762451.jpg?v=1592395482</image:loc>
      <image:title>Cytochrome P450 2A6 Antibody</image:title>
      <image:caption>DF3572 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3573</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2720_thumb_P_1523425680851.jpg?v=1592395479</image:loc>
      <image:title>Cytochrome P450 2A13 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using Cytochrome P450 2A13 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3574</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2721_thumb_P_1418200809469.jpg?v=1592395477</image:loc>
      <image:title>Cytochrome P450 2B6 Antibody</image:title>
      <image:caption>DF3574 staining HT29  cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3575</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2722_thumb_P_1418200871802.jpg?v=1592395475</image:loc>
      <image:title>Cytochrome P450 2C8 Antibody</image:title>
      <image:caption>DF3575 at 1/100 staining Human cervical cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3576</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2723_thumb_P_1418200908603.jpg?v=1592395473</image:loc>
      <image:title>Cytochrome P450 2C8/9/18/19 Antibody</image:title>
      <image:caption>DF3576 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3577</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2724_thumb_P_1418200923249.jpg?v=1592395471</image:loc>
      <image:title>Cytochrome P450 2D6 Antibody</image:title>
      <image:caption>DF3577 staining  HT29 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3578</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2725_thumb_P_1418200959522.jpg?v=1592395469</image:loc>
      <image:title>Cytochrome P450 2E1 Antibody</image:title>
      <image:caption>DF3578 at 1/100 staining Human cervical cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3579</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2726_thumb_P_1505179216485.jpg?v=1592395467</image:loc>
      <image:title>Cytochrome P450 2J2 Antibody</image:title>
      <image:caption>DF3579 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3580</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2727_thumb_P_1418200998004.jpg?v=1592395465</image:loc>
      <image:title>Cytochrome P450 2R1 Antibody</image:title>
      <image:caption>DF3580 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3581</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2728_thumb_P_1418201019993.jpg?v=1592395463</image:loc>
      <image:title>Cytochrome P450 2S1 Antibody</image:title>
      <image:caption>DF3581 at 1/100 staining Human lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3582</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2729_thumb_P_1418201039277.jpg?v=1592395461</image:loc>
      <image:title>Cytochrome P450 2U1 Antibody</image:title>
      <image:caption>DF3582 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3583</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2730_thumb_P_1418201059417.jpg?v=1592395459</image:loc>
      <image:title>Cytochrome P450 2W1 Antibody</image:title>
      <image:caption>DF3583 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3584</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2731_thumb_P_1418201112208.jpg?v=1592395457</image:loc>
      <image:title>Cytochrome P450 3A43 Antibody</image:title>
      <image:caption>DF3584 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3585</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2732_thumb_P_1418201132441.jpg?v=1592395454</image:loc>
      <image:title>Cytochrome P450 39A1 Antibody</image:title>
      <image:caption>DF3585 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3586</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2733_thumb_P_1501467930690.jpg?v=1592395452</image:loc>
      <image:title>Cytochrome P450 3A4/5 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using Cytochrome P450 3A4/5 Antibody. Lane 1: Hela  treated with  blocking peptide; Lane 2: Hela; Lane 3: rat brain; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3587</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2734_thumb_P_1505179284996.jpg?v=1592395450</image:loc>
      <image:title>Cytochrome P450 3A4 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat heart, using Cytochrome P450 3A4 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3588</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2735_thumb_P_1505179315957.jpg?v=1592395448</image:loc>
      <image:title>Cytochrome P450 4B1 Antibody</image:title>
      <image:caption>DF3588 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3589</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2736_thumb_P_1505179351711.jpg?v=1592395446</image:loc>
      <image:title>Cytochrome P450 4X1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from VERO, using Cytochrome P450 4X1 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3590</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2737_thumb_P_1496377136554.jpg?v=1592395444</image:loc>
      <image:title>Cytochrome P450 4Z1 Antibody</image:title>
      <image:caption>DF3590 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3591</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2738_thumb_P_1505976442148.jpg?v=1592395443</image:loc>
      <image:title>Cytochrome P450 51A1 Antibody</image:title>
      <image:caption>Western blot analysis of Cytochrome P450 51A1 using A431 whole cell lysates</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3592</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2739_thumb_P_1418201395583.jpg?v=1592395437</image:loc>
      <image:title>Cytochrome P450 7B1 Antibody</image:title>
      <image:caption>DF3592 staining LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3593</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2740_thumb_P_1406634057736.jpg?v=1592395435</image:loc>
      <image:title>CYTL1 Antibody</image:title>
      <image:caption>DF3593 at 1/100 staining Human Melanoma tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3594</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2741_thumb_P_1499427456004.jpg?v=1592395433</image:loc>
      <image:title>DNAJB4 Antibody</image:title>
      <image:caption>DF3594 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3595</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2742_thumb_P_1529920347865.jpg?v=1592395431</image:loc>
      <image:title>FGF18 Antibody</image:title>
      <image:caption>DF3595 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3596</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2743_thumb_P_1501467996009.jpg?v=1592395429</image:loc>
      <image:title>FGF23 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using FGF23 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3597</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2744_thumb_P_1418201424874.jpg?v=1592395428</image:loc>
      <image:title>FRS3 Antibody</image:title>
      <image:caption>DF3597 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3598</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2745_thumb_P_1418201453014.jpg?v=1592395426</image:loc>
      <image:title>GBP1 Antibody</image:title>
      <image:caption>DF3598 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3599</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2746_thumb_P_1418201475176.jpg?v=1592395424</image:loc>
      <image:title>GRID1 Antibody</image:title>
      <image:caption>DF3599 at 1/100 staining Mouse intestine tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3600</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2747_thumb_P_1527501287709.jpg?v=1592395421</image:loc>
      <image:title>GRID2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using GRID2 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3601</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2748_thumb_P_1523769006550.jpg?v=1592395420</image:loc>
      <image:title>HSPB2 Antibody</image:title>
      <image:caption>DF3601 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3602</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2749_thumb_P_1418201494620.jpg?v=1592395418</image:loc>
      <image:title>IL17RA Antibody</image:title>
      <image:caption>DF3602 staining LOVO by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3603</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2750_thumb_P_1527501287818.jpg?v=1592395416</image:loc>
      <image:title>IL20RB Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using IL20RB Antibody. Lane 1: HepG2  treated with  blocking peptide; Lane 2: HepG2; Lane 3: mouse spleen; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3604</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2751_thumb_P_1505179384567.jpg?v=1592395414</image:loc>
      <image:title>MAPK9 Antibody</image:title>
      <image:caption>DF3604 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3605</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2752_thumb_P_1418201530621.jpg?v=1592395412</image:loc>
      <image:title>BARD1 Antibody</image:title>
      <image:caption>DF3605 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3606</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2753_thumb_P_1529777053081.jpg?v=1592395410</image:loc>
      <image:title>BCL10 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using BCL10 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3607</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2754_thumb_P_1406634058455.jpg?v=1592395408</image:loc>
      <image:title>BCLW Antibody</image:title>
      <image:caption>DF3607 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3608</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2755_thumb_P_1406634058225.jpg?v=1592395406</image:loc>
      <image:title>CIDEB Antibody</image:title>
      <image:caption>DF3608 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3609</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2756_thumb_P_1406634058281.jpg?v=1592395404</image:loc>
      <image:title>CYB5 Antibody</image:title>
      <image:caption>DF3609 staining A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3610</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2757_thumb_P_1418201552706.jpg?v=1592395402</image:loc>
      <image:title>DAXX Antibody</image:title>
      <image:caption>DF3610 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3611</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2758_thumb_P_1406634058973.jpg?v=1592395400</image:loc>
      <image:title>DCC Antibody</image:title>
      <image:caption>DF3611 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3612</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2759_thumb_P_1406634058115.jpg?v=1592395398</image:loc>
      <image:title>DIDO1 Antibody</image:title>
      <image:caption>DF3612 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3613</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2760_thumb_P_1406634058715.jpg?v=1592395396</image:loc>
      <image:title>DNL4 Antibody</image:title>
      <image:caption>DF3613 staining HepG2? cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3614</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2761_thumb_P_1418201568483.jpg?v=1592395394</image:loc>
      <image:title>ELOA3 Antibody</image:title>
      <image:caption>DF3614 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3615</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2762_thumb_P_1418201600642.jpg?v=1592395392</image:loc>
      <image:title>EXO1 Antibody</image:title>
      <image:caption>DF3615 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3616</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2763_thumb_P_1418201627101.jpg?v=1592395390</image:loc>
      <image:title>EIF4G2 Antibody</image:title>
      <image:caption>DF3616 staining A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3617</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2764_thumb_P_1406634058869.jpg?v=1592395388</image:loc>
      <image:title>LAMA4 Antibody</image:title>
      <image:caption>DF3617 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3618</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2765_thumb_P_1406634058170.jpg?v=1592395386</image:loc>
      <image:title>LAMB1 Antibody</image:title>
      <image:caption>DF3618 at 1/100 staining Human uterus tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3619</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2766_thumb_P_1406634058912.jpg?v=1592395383</image:loc>
      <image:title>LAMC1 Antibody</image:title>
      <image:caption>DF3619 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3620</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2767_thumb_P_1406634058554.jpg?v=1592395381</image:loc>
      <image:title>MGMT Antibody</image:title>
      <image:caption>DF3620 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3621</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2768_thumb_P_1527501298914.jpg?v=1592395379</image:loc>
      <image:title>MLH1 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from mouse lung, using MLH1 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3622</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2769_thumb_P_1500637746103.jpg?v=1592395378</image:loc>
      <image:title>MLH3 Antibody</image:title>
      <image:caption>DF3622 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3623</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2770_thumb_P_1418201701487.jpg?v=1592395376</image:loc>
      <image:title>MRE11A Antibody</image:title>
      <image:caption>DF3623 staining  NIH-3T3 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3624</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2771_thumb_P_1406634058737.jpg?v=1592395374</image:loc>
      <image:title>MSH3 Antibody</image:title>
      <image:caption>DF3624 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3625</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2772_thumb_P_1527501298068.jpg?v=1592395371</image:loc>
      <image:title>PARP2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 3T3, using PARP2 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3626</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2773_thumb_P_1406634058791.jpg?v=1592395370</image:loc>
      <image:title>PHLA1 Antibody</image:title>
      <image:caption>DF3626 staining  RAW264.7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3627</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2774_thumb_P_1418201830430.jpg?v=1592395368</image:loc>
      <image:title>PMS2 Antibody</image:title>
      <image:caption>DF3627 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3628</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2775_thumb_P_1505179431873.jpg?v=1592395366</image:loc>
      <image:title>PRPF19 Antibody</image:title>
      <image:caption>DF3628 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3629</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2776_thumb_P_1406634058768.jpg?v=1592395364</image:loc>
      <image:title>RAD51L1 Antibody</image:title>
      <image:caption>DF3629 at 1/100 staining Human brain tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3630</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2777_thumb_P_1406634058119.jpg?v=1592395362</image:loc>
      <image:title>RAD51L3 Antibody</image:title>
      <image:caption>DF3630 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3631</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2778_thumb_P_1418201891355.jpg?v=1592395359</image:loc>
      <image:title>RAD54 Antibody</image:title>
      <image:caption>DF3631 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3632</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2779_thumb_P_1505179462029.jpg?v=1592395357</image:loc>
      <image:title>RAD23A Antibody</image:title>
      <image:caption>Western blot analysis of extracts from LOVO cells, using RAD23A antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3633</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2780_thumb_P_1500637820650.jpg?v=1592395356</image:loc>
      <image:title>T3JAM Antibody</image:title>
      <image:caption>DF3633 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3634</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2781_thumb_P_1406634058690.jpg?v=1592395354</image:loc>
      <image:title>WWOX Antibody</image:title>
      <image:caption>DF3634 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3635</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2782_thumb_P_1523769006346.jpg?v=1592395352</image:loc>
      <image:title>STAT5A/B Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using STAT5A/B Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3636</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2783_thumb_P_1406634059322.jpg?v=1592395337</image:loc>
      <image:title>KLF7 Antibody</image:title>
      <image:caption>DF3636 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3637</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2784_thumb_P_1406634059776.jpg?v=1592395334</image:loc>
      <image:title>ORC1L Antibody</image:title>
      <image:caption>DF3637 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3638</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2785_thumb_P_1499427550608.jpg?v=1592395332</image:loc>
      <image:title>POU4F3 Antibody</image:title>
      <image:caption>DF3638 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3639</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2786_thumb_P_1406634059873.jpg?v=1592395330</image:loc>
      <image:title>EFTUD2 Antibody</image:title>
      <image:caption>DF3639 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3640</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2787_thumb_P_1523425680995.jpg?v=1592395328</image:loc>
      <image:title>AGPAT4 Antibody</image:title>
      <image:caption>DF3640 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3641</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2788_thumb_P_1527501277342.jpg?v=1592395326</image:loc>
      <image:title>AGPAT5 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using AGPAT5 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3642</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2789_thumb_P_1527501277393.jpg?v=1592395324</image:loc>
      <image:title>AGPAT3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Mouse cancer, using AGPAT3 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3643</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2790_thumb_P_1406634059686.jpg?v=1592395321</image:loc>
      <image:title>PSMD11 Antibody</image:title>
      <image:caption>DF3643 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3644</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2791_thumb_P_1505179490893.jpg?v=1592395319</image:loc>
      <image:title>PSMD12 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using PSMD12 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3645</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2792_thumb_P_1418201937756.jpg?v=1592395317</image:loc>
      <image:title>PSMD3 Antibody</image:title>
      <image:caption>DF3645 at 1/100 staining Mouse spleen tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3646</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2793_thumb_P_1406634059917.jpg?v=1592395315</image:loc>
      <image:title>MRPS12 Antibody</image:title>
      <image:caption>DF3646 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3647</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2794_thumb_P_1406634059341.jpg?v=1592395313</image:loc>
      <image:title>MRPS16 Antibody</image:title>
      <image:caption>DF3647 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3648</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2795_thumb_P_1406634059089.jpg?v=1592395311</image:loc>
      <image:title>MRPS17 Antibody</image:title>
      <image:caption>DF3648 staining NIH-3T3 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3649</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2796_thumb_P_1406634059315.jpg?v=1592395309</image:loc>
      <image:title>MRPS18C Antibody</image:title>
      <image:caption>DF3649 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3650</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2797_thumb_P_1406634059003.jpg?v=1592395306</image:loc>
      <image:title>MRPS35 Antibody</image:title>
      <image:caption>DF3650 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3651</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2798_thumb_P_1406634059851.jpg?v=1592395304</image:loc>
      <image:title>MRPS7 Antibody</image:title>
      <image:caption>DF3651 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3652</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2799_thumb_P_1406634059958.jpg?v=1592395302</image:loc>
      <image:title>MRPS9 Antibody</image:title>
      <image:caption>DF3652 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3653</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2800_thumb_P_1523425680504.jpg?v=1592395300</image:loc>
      <image:title>HSD3B7 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using HSD3B7 Antibody. Lane 1: 293  treated with  blocking peptide; Lane 2: 293; Lane 3: HepG2; </image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3654</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2801_thumb_P_1406634059253.jpg?v=1592395298</image:loc>
      <image:title>MRPL54 Antibody</image:title>
      <image:caption>DF3654 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3655</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2802_thumb_P_1498711710245.jpg?v=1592395296</image:loc>
      <image:title>MRPL10 Antibody</image:title>
      <image:caption>DF3655 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3656</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2803_thumb_P_1505179521903.jpg?v=1592395294</image:loc>
      <image:title>MRPL11 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293 and hela and rat brain, using MRPL11 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3657</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2804_thumb_P_1406634059340.jpg?v=1592395292</image:loc>
      <image:title>MRPL12 Antibody</image:title>
      <image:caption>DF3657 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3658</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2805_thumb_P_1498711781331.jpg?v=1592395290</image:loc>
      <image:title>MRPL13 Antibody</image:title>
      <image:caption>DF3658 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3659</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2806_thumb_P_1525743842869.jpg?v=1592395288</image:loc>
      <image:title>MRPL14 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MRPL14 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3660</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2807_thumb_P_1525743842170.jpg?v=1592395284</image:loc>
      <image:title>MRPL15 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MRPL15 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3661</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2808_thumb_P_1498625581017.jpg?v=1592395283</image:loc>
      <image:title>MRPL16 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MRPL16 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3662</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2809_thumb_P_1406634059134.jpg?v=1592395280</image:loc>
      <image:title>MRPL18 Antibody</image:title>
      <image:caption>DF3662 staining HT29 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3663</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2810_thumb_P_1501468134553.jpg?v=1592395278</image:loc>
      <image:title>MRPL20 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain, using MRPL20 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3664</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2811_thumb_P_1406634059596.jpg?v=1592395276</image:loc>
      <image:title>MRPL21 Antibody</image:title>
      <image:caption>DF3664 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3665</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2812_thumb_P_1406634060904.jpg?v=1592395274</image:loc>
      <image:title>MRPL22 Antibody</image:title>
      <image:caption>DF3665 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3666</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2813_thumb_P_1406634060767.jpg?v=1592395272</image:loc>
      <image:title>MRPL24 Antibody</image:title>
      <image:caption>DF3666 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3667</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2814_thumb_P_1525743842713.jpg?v=1592395270</image:loc>
      <image:title>MRPL32 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using MRPL32 Antibody. Lane 1 was treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3668</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2815_thumb_P_1406634060780.jpg?v=1592395268</image:loc>
      <image:title>MRPL35 Antibody</image:title>
      <image:caption>DF3668 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3669</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2816_thumb_P_1406634060993.jpg?v=1592395266</image:loc>
      <image:title>MRPL40 Antibody</image:title>
      <image:caption>DF3669 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3670</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2817_thumb_P_1406634060991.jpg?v=1592395263</image:loc>
      <image:title>MRPL41 Antibody</image:title>
      <image:caption>DF3670 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3671</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2818_thumb_P_1527501297831.jpg?v=1592395261</image:loc>
      <image:title>MRPL44 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using MRPL44 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3672</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2819_thumb_P_1406634060505.jpg?v=1592395259</image:loc>
      <image:title>MRPL46 Antibody</image:title>
      <image:caption>DF3672 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3673</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2820_thumb_P_1406634060710.jpg?v=1592395257</image:loc>
      <image:title>MRPL47 Antibody</image:title>
      <image:caption>DF3673 staining RAW264.7 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3674</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2821_thumb_P_1406634060740.jpg?v=1592395254</image:loc>
      <image:title>MRPL51 Antibody</image:title>
      <image:caption>DF3674 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3675</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2822_thumb_P_1406634060312.jpg?v=1592395252</image:loc>
      <image:title>MRPL9 Antibody</image:title>
      <image:caption>DF3675 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3676</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2823_thumb_P_1406634060816.jpg?v=1592395245</image:loc>
      <image:title>RPS11 Antibody</image:title>
      <image:caption>DF3676 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3677</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2824_thumb_P_1406634060319.jpg?v=1592395243</image:loc>
      <image:title>RPS12 Antibody</image:title>
      <image:caption>DF3677 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3678</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2825_thumb_P_1406634060653.jpg?v=1592395241</image:loc>
      <image:title>RPS15 Antibody</image:title>
      <image:caption>DF3678 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3679</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2826_thumb_P_1505179615191.jpg?v=1592395239</image:loc>
      <image:title>RPS18 Antibody</image:title>
      <image:caption>DF3679 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3680</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2664_thumb_P_1530178115017.jpg?v=1592395238</image:loc>
      <image:title>RPS19 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2 and 293, using RPS19 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3681</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2665_thumb_P_1406634055183.jpg?v=1592395236</image:loc>
      <image:title>RPS20 Antibody</image:title>
      <image:caption>DF3681 staining  HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3682</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2666_thumb_P_1406634055707.jpg?v=1592395234</image:loc>
      <image:title>RPS23 Antibody</image:title>
      <image:caption>DF3682 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3683</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2667_thumb_P_1406634055110.jpg?v=1592395232</image:loc>
      <image:title>RPS27L Antibody</image:title>
      <image:caption>DF3683 staining  COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3684</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2668_thumb_P_1527501266321.jpg?v=1592395230</image:loc>
      <image:title>RPS3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using RPS3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3685</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2669_thumb_P_1498711851671.jpg?v=1592395228</image:loc>
      <image:title>RPS4X Antibody</image:title>
      <image:caption>DF3685 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3686</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2670_thumb_P_1523769006965.jpg?v=1592395226</image:loc>
      <image:title>RPS4Y1 Antibody</image:title>
      <image:caption>DF3686 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3687</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2671_thumb_P_1523768996542.jpg?v=1592395225</image:loc>
      <image:title>RPS5 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using RPS5 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3688</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2827_thumb_P_1406634060545.jpg?v=1592395223</image:loc>
      <image:title>RPS7 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from JurKat cells using RPS7 antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3689</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2828_thumb_P_1406634060600.jpg?v=1592395221</image:loc>
      <image:title>RPS8 Antibody</image:title>
      <image:caption>DF3689 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3690</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2829_thumb_P_1406634060058.jpg?v=1592395219</image:loc>
      <image:title>RPS9 Antibody</image:title>
      <image:caption>DF3690 staining  HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3691</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2830_thumb_P_1406634060843.jpg?v=1592395217</image:loc>
      <image:title>PRKAG1 Antibody</image:title>
      <image:caption>DF3691 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3692</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2831_thumb_P_1406634060548.jpg?v=1592395214</image:loc>
      <image:title>AZI1 Antibody</image:title>
      <image:caption>DF3692 at 1/100 staining Human cervical cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3693</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2832_thumb_P_1418201957298.jpg?v=1592395212</image:loc>
      <image:title>TROVE2 Antibody</image:title>
      <image:caption>DF3693 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3694</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2833_thumb_P_1406634061776.jpg?v=1592395210</image:loc>
      <image:title>RPL10A Antibody</image:title>
      <image:caption>DF3694 staining  HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3695</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2834_thumb_P_1406634061003.jpg?v=1592395208</image:loc>
      <image:title>RPL10L Antibody</image:title>
      <image:caption>DF3695 staining  Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3696</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2835_thumb_P_1505179670583.jpg?v=1592395206</image:loc>
      <image:title>RPL11 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Rat  brain, using RPL11 Antibody. The lane on the left was treated with blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3697</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2836_thumb_P_1406634061127.jpg?v=1592395204</image:loc>
      <image:title>RPL12 Antibody</image:title>
      <image:caption>DF3697 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3698</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2837_thumb_P_1499428039559.jpg?v=1592395202</image:loc>
      <image:title>RPL15 Antibody</image:title>
      <image:caption>DF3698 staining  LOVO cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3699</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2838_thumb_P_1501468201720.jpg?v=1592395201</image:loc>
      <image:title>RPL17 Antibody</image:title>
      <image:caption>DF3699 at 1/100 staining Rat kidney tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3700</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2839_thumb_P_1523768995446.jpg?v=1592395199</image:loc>
      <image:title>RPL18 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using RPL18 Antibody.
 Lane 1: COS-7, treated with blocking peptide;
 Lane 2: COS-7;
 Lane 3: MCF7.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3701</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/df3701_rpl19_antibody_thumb_P_1544408468426.jpg?v=1592395197</image:loc>
      <image:title>RPL19 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using RPL19 Antibody.
 Lane 1: Rat  brain, treated with blocking peptide;
 Lane 2: Rat  brain;
 Lane 3: Hybridoma cells;
 Lane 4: Mouse  lung;
 Lane 5: 293.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3702</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2841_thumb_P_1406634061974.jpg?v=1592395195</image:loc>
      <image:title>RPL23 Antibody</image:title>
      <image:caption>DF3702 at 1/100 staining Rat spleen tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3703</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2842_thumb_P_1406634061168.jpg?v=1592395193</image:loc>
      <image:title>RPL26L Antibody</image:title>
      <image:caption>DF3703 staining HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3704</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2843_thumb_P_1523425666653.jpg?v=1592395191</image:loc>
      <image:title>RPL27A Antibody</image:title>
      <image:caption>DF3704 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3705</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2844_thumb_P_1523425642989.jpg?v=1592395189</image:loc>
      <image:title>RPL28 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from various samples, using RPL28 Antibody.
 Lane 1: COS-7, treated with blocking peptide;
 Lane 2: COS-7;
 Lane 3: MCF7;
 Lane 4: Hela;
 Lane 5: Hybridoma cells.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3706</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2845_thumb_P_1523768996756.jpg?v=1592395188</image:loc>
      <image:title>RPL3 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using RPL3 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3707</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2846_thumb_P_1406634061803.jpg?v=1592395186</image:loc>
      <image:title>RPL30 Antibody</image:title>
      <image:caption>DF3707 at 1/100 staining Human lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3708</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2847_thumb_P_1498267496508.jpg?v=1592395184</image:loc>
      <image:title>RPL34 Antibody</image:title>
      <image:caption>DF3708 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3709</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2848_thumb_P_1499428238358.jpg?v=1592395182</image:loc>
      <image:title>RPL35 Antibody</image:title>
      <image:caption>DF3709 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3710</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2849_thumb_P_1523769006139.jpg?v=1592395181</image:loc>
      <image:title>RPL36 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from HepG2, using RPL36 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3711</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2850_thumb_P_1529319712606.jpg?v=1592395179</image:loc>
      <image:title>RPL39 Antibody</image:title>
      <image:caption>DF3711 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3712</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2851_thumb_P_1523768996023.jpg?v=1592395177</image:loc>
      <image:title>RPL5 Antibody</image:title>
      <image:caption>DF3712 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3713</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2852_thumb_P_1406634062951.jpg?v=1592395176</image:loc>
      <image:title>RPL7 Antibody</image:title>
      <image:caption>DF3713 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3714</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2853_thumb_P_1406634062926.jpg?v=1592395174</image:loc>
      <image:title>PGD Antibody</image:title>
      <image:caption>DF3714 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3715</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2854_thumb_P_1406634062209.jpg?v=1592395172</image:loc>
      <image:title>PGLS Antibody</image:title>
      <image:caption>DF3715 at 1/100 staining Human prostate tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3716</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2855_thumb_P_1406634062187.jpg?v=1592395170</image:loc>
      <image:title>ABHD11 Antibody</image:title>
      <image:caption>DF3716 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3717</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2856_thumb_P_1406634062721.jpg?v=1592395168</image:loc>
      <image:title>ABHD12 Antibody</image:title>
      <image:caption>DF3717 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3718</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2857_thumb_P_1406634062155.jpg?v=1592395166</image:loc>
      <image:title>ABHD14A Antibody</image:title>
      <image:caption>DF3718 staining  RAW264.7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3719</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2858_thumb_P_1500637950529.jpg?v=1592395164</image:loc>
      <image:title>ABHD2 Antibody</image:title>
      <image:caption>DF3719 staining HT29 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3720</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2859_thumb_P_1406634062161.jpg?v=1592395162</image:loc>
      <image:title>ABHD6 Antibody</image:title>
      <image:caption>DF3720 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3721</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3722</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2861_thumb_P_1523768994590.jpg?v=1592395154</image:loc>
      <image:title>ABHD8 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using ABHD8 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3723</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2862_thumb_P_1406634062383.jpg?v=1592395153</image:loc>
      <image:title>ABHD9 Antibody</image:title>
      <image:caption>DF3723 staining  MCF7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3724</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2863_thumb_P_1418202003828.jpg?v=1592395151</image:loc>
      <image:title>CHRNB1 Antibody</image:title>
      <image:caption>DF3724 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3725</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2864_thumb_P_1418202028696.jpg?v=1592395148</image:loc>
      <image:title>ACHE Antibody</image:title>
      <image:caption>DF3725 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3726</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2865_thumb_P_1499428626120.jpg?v=1592395146</image:loc>
      <image:title>ACAT1 Antibody</image:title>
      <image:caption>DF3726 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3727</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2866_thumb_P_1418202045839.jpg?v=1592395145</image:loc>
      <image:title>ACSS1 Antibody</image:title>
      <image:caption>DF3727 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3728</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2867_thumb_P_1499428843222.jpg?v=1592395142</image:loc>
      <image:title>ACSA Antibody</image:title>
      <image:caption>Western blot analysis of extracts of various tissue ,using ACSA antibody</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3729</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2868_thumb_P_1506479670390.jpg?v=1592395140</image:loc>
      <image:title>SLC33A1 Antibody</image:title>
      <image:caption>Western blot analysis of SLC33A1 expression in Human Placenta lysate</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3730</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2869_thumb_P_1406634062604.jpg?v=1592395138</image:loc>
      <image:title>ANP32B Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat brain cells, using ANP32B antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3731</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2870_thumb_P_1505179700453.jpg?v=1592395136</image:loc>
      <image:title>ACTR3 Antibody</image:title>
      <image:caption>DF3731 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3732</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2871_thumb_P_1406634062970.jpg?v=1592395134</image:loc>
      <image:title>ACBD6 Antibody</image:title>
      <image:caption>DF3732 staining HepG2 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3733</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2872_thumb_P_1406634062550.jpg?v=1592395132</image:loc>
      <image:title>ACOT1 Antibody</image:title>
      <image:caption>DF3733 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3734</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2873_thumb_P_1418202072532.jpg?v=1592395130</image:loc>
      <image:title>ACOT2 Antibody</image:title>
      <image:caption>DF3734 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3735</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2874_thumb_P_1498268643074.jpg?v=1592395128</image:loc>
      <image:title>ACOT4 Antibody</image:title>
      <image:caption>DF3735 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3736</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2875_thumb_P_1406634062229.jpg?v=1592395126</image:loc>
      <image:title>ACOT8 Antibody</image:title>
      <image:caption>DF3736 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3737</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2876_thumb_P_1406634062595.jpg?v=1592395124</image:loc>
      <image:title>LYPLA1 Antibody</image:title>
      <image:caption>DF3737 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3738</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2877_thumb_P_1505179747425.jpg?v=1592395122</image:loc>
      <image:title>LPCAT2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from rat heart, using LPCAT2 Antibody. Lane 1 was treated with the blocking peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3739</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2878_thumb_P_1505179819487.jpg?v=1592395120</image:loc>
      <image:title>ADAM32 Antibody</image:title>
      <image:caption>DF3739 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3740</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2879_thumb_P_1406634062471.jpg?v=1592395118</image:loc>
      <image:title>ADAMTS18 Antibody</image:title>
      <image:caption>DF3740 staining  NIH-3T3 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3741</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2880_thumb_P_1526892891519.jpg?v=1592395117</image:loc>
      <image:title>ADAMTS19 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from Hela, using ADAMTS19 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3742</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2881_thumb_P_1527501296436.jpg?v=1592395115</image:loc>
      <image:title>SLC25A6 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from 293, using SLC25A6 Antibody.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3743</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2882_thumb_P_1498268250332.jpg?v=1592395113</image:loc>
      <image:title>SLC25A31 Antibody</image:title>
      <image:caption>DF3743 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3744</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2883_thumb_P_1500638036941.jpg?v=1592395111</image:loc>
      <image:title>BST1 Antibody</image:title>
      <image:caption>DF3744 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3745</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2884_thumb_P_1523375501710.jpg?v=1592395109</image:loc>
      <image:title>ARF4 Antibody</image:title>
      <image:caption>DF3745 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3746</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2885_thumb_P_1505179872896.jpg?v=1592395108</image:loc>
      <image:title>ARF6 Antibody</image:title>
      <image:caption>DF3746 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3747</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2886_thumb_P_1418202088589.jpg?v=1592395106</image:loc>
      <image:title>ARFGAP1 Antibody</image:title>
      <image:caption>DF3747 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3748</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2887_thumb_P_1505179944671.jpg?v=1592395104</image:loc>
      <image:title>ARFGAP3 Antibody</image:title>
      <image:caption>DF3748 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3749</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2888_thumb_P_1406634063643.jpg?v=1592395102</image:loc>
      <image:title>ARL2BP Antibody</image:title>
      <image:caption>DF3749 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3750</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2889_thumb_P_1505179981495.jpg?v=1592395100</image:loc>
      <image:title>AGXT2L2 Antibody</image:title>
      <image:caption>DF3750 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3751</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2890_thumb_P_1406634063296.jpg?v=1592395098</image:loc>
      <image:title>AARSD1 Antibody</image:title>
      <image:caption>DF3751 staining A549 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3752</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2891_thumb_P_1505180053731.jpg?v=1592395096</image:loc>
      <image:title>AKR1A1 Antibody</image:title>
      <image:caption>DF3752 staining COLO205 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3753</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2892_thumb_P_1406634063639.jpg?v=1592395094</image:loc>
      <image:title>ADH7 Antibody</image:title>
      <image:caption>DF3753 staining Hela cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3754</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2893_thumb_P_1418202114373.jpg?v=1592395092</image:loc>
      <image:title>ALDH3B1 Antibody</image:title>
      <image:caption>DF3754 at 1/100 staining Human lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3755</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2894_thumb_P_1418202143415.jpg?v=1592395090</image:loc>
      <image:title>ALDH1B1 Antibody</image:title>
      <image:caption>DF3755 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3756</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2895_thumb_P_1406634063781.jpg?v=1592395088</image:loc>
      <image:title>AOX1 Antibody</image:title>
      <image:caption>DF3756 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3757</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2896_thumb_P_1406634063645.jpg?v=1592395086</image:loc>
      <image:title>AKR1C2 Antibody</image:title>
      <image:caption>DF3757 staining COLO205 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3758</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2897_thumb_P_1499429052474.jpg?v=1592395083</image:loc>
      <image:title>AKR1CL2 Antibody</image:title>
      <image:caption>DF3758 staining  A549 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3759</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2898_thumb_P_1406634063830.jpg?v=1592395082</image:loc>
      <image:title>AKR1B1 Antibody</image:title>
      <image:caption>DF3759 staining  HuvEc cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3760</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2899_thumb_P_1406634063511.jpg?v=1592395079</image:loc>
      <image:title>ASAH3L Antibody</image:title>
      <image:caption>DF3760 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3761</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2900_thumb_P_1406634063145.jpg?v=1592395077</image:loc>
      <image:title>PHCA Antibody</image:title>
      <image:caption>DF3761 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3762</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2901_thumb_P_1406634063747.jpg?v=1592395075</image:loc>
      <image:title>A4GNT Antibody</image:title>
      <image:caption>DF3762 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3763</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2902_thumb_P_1406634063143.jpg?v=1592395073</image:loc>
      <image:title>AASS Antibody</image:title>
      <image:caption>DF3763 staining 293 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3764</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2903_thumb_P_1499429126871.jpg?v=1592395071</image:loc>
      <image:title>SGCA Antibody</image:title>
      <image:caption>DF3764 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3765</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2904_thumb_P_1418202163642.jpg?v=1592395070</image:loc>
      <image:title>SCNN1D Antibody</image:title>
      <image:caption>DF3765 staining RAW264.7 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3766</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2905_thumb_P_1406634063271.jpg?v=1592395064</image:loc>
      <image:title>AMPD2 Antibody</image:title>
      <image:caption>DF3766 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3767</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2906_thumb_P_1418202189028.jpg?v=1592395062</image:loc>
      <image:title>AMPH Antibody</image:title>
      <image:caption>DF3767 staining HeLa cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3768</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2907_thumb_P_1418202206603.jpg?v=1592395061</image:loc>
      <image:title>APBA3 Antibody</image:title>
      <image:caption>DF3768 staining HuvEc by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3769</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2908_thumb_P_1418202240823.jpg?v=1592395058</image:loc>
      <image:title>APBB2 Antibody</image:title>
      <image:caption>DF3769 at 1/100 staining Rat heart tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3770</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2909_thumb_P_1406634063886.jpg?v=1592395057</image:loc>
      <image:title>NECAB3 Antibody</image:title>
      <image:caption>DF3770 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3771</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2910_thumb_P_1500638121600.jpg?v=1592395054</image:loc>
      <image:title>APPBP2 Antibody</image:title>
      <image:caption>DF3771 staining  293 cells by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3772</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2911_thumb_P_1418202318608.jpg?v=1592395053</image:loc>
      <image:title>APLP2 Antibody</image:title>
      <image:caption>Western blot analysis of extracts from A549 cells using APLP2 antibody.The lane on the left is treated with the antigen-specific peptide.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3773</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2672_thumb_P_1418202337114.jpg?v=1592395051</image:loc>
      <image:title>ALS2CR11 Antibody</image:title>
      <image:caption>DF3773 staining NIH-3T3 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3774</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2673_thumb_P_1505180087246.jpg?v=1592395049</image:loc>
      <image:title>ALS2CR4 Antibody</image:title>
      <image:caption>DF3774 staining Hela by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod</image:caption>
    </image:image>
  </url>
  <url>
    <loc>https://www.phscientific.com/products/df3775</loc>
    <lastmod>2026-07-22T08:33:55+12:00</lastmod>
    <changefreq>daily</changefreq>
    <image:image>
      <image:loc>https://cdn.shopify.com/s/files/1/0286/4418/0061/products/2674_thumb_P_1499429213493.jpg?v=1592395047</image:loc>
      <image:title>ALS2CR8 Antibody</image:title>
      <image:caption>DF3775 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary</image:caption>
    </image:image>
  </url>
</urlset>
