Antibodies

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Western blot analysis of extracts from various samples, using K1H2 Antibody.
 Lane 1: 293 treated with blocking peptide.
 Lane 2: 293;
 Lane 3: Rat lung,Hela;
DF9002 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
Western blot analysis of extracts from various samples, using Keratin 9 Antibody.
 Lane 1: Rat heart treated with blocking peptide;
 Lane 2: Rat heart;
 Lane 3: Hela.
DF9000 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
Western blot analysis of JAM3 using K562 whole cell lysates
Western blot analysis of KDM5A using LOVO whole cell lysates
Western blot analysis ITFG2 using NIH-3T3 whole cell lysates
Western blot analysis ITBP2 using Jurkat whole cell lysates
Western blot analysis ITGAD using COLO205 whole cell lysates
Western blot analysis ITGA9 using K562 whole cell lysates
Western blot analysis ITGA8 using LOVO whole cell lysates
Western blot analysis ITGA11 using A549 whole cell lysates
Western blot analysis of extracts from Hela, using INSL5 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis INSIG2 using HeLa whole cell lysates
Western blot analysis IFI27 using Jurkat whole cell lysates
Western blot analysis INGR2 using HeLa whole cell lysates
Western blot analysis ILRL2 using HuvEc whole cell lysates
Western blot analysis IL31 using HT29 whole cell lysates
DF8985 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
DF9146 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
DF9145 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
Western blot analysis of extracts from Mouse muscle, using CHRNG Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from Mouse brain, using ABHD3 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from Mouse brain, using ABHD13 Antibody. Lane 1 was treated with the blocking peptide.

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