Antibodies

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Western blot analysis of CLDN9 using COLO205 whole cell lysates
DF9395 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
Western blot analysis of extracts from HepG2 and rat muscle , using CLDN22/24 Antibody.
Western blot analysis of extracts from rat brain, using CLDN20 Antibody.
Western blot analysis of extracts from various samples, using CLDN18 Antibody.
 Lane 1: COS-7, treated with blocking peptide;
 Lane 2: COS-7;
 Lane 3: 3T3.
DF9391 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
Western blot analysis of CLDN12 using K562 whole cell lysates
DF9389 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
DF9388 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
Western blot analysis of CMTM5 using HeLa whole cell lysates
Western blot analysis of LUC7L3 using Jurkat whole cell lysates
DF9385 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
DF9384 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
Western blot analysis of extracts from rat brain, using CHD8 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of CHD6 using MCF7 whole cell lysates
Western blot analysis of CHD2 using HT29 whole cell lysates
Western blot analysis of CBX2 using 293 whole cell lysates
Western blot analysis SLC18A1 using LOVO whole cell lysates
Western blot analysis of extracts from rat brain, mouse brain, using CHSY3 Antibody.
Western blot analysis of CLCN1 using K562 whole cell lysates
Western blot analysis of CLCNKB using COLO205 whole cell lysates
Western blot analysis of CLCN2 using K562 whole cell lysates
DF9374 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
Western blot analysis of PDE5A using HuvEc whole cell lysates

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