Antibodies

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Western blot analysis of extracts from mouse brain, using CTNND2 Antibody.
Western blot analysis of CTNNA2 using COLO205 whole cell lysates
Western blot analysis of CEACAM7 using Jurkat whole cell lysates
DF9345 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 Mouse brain, using CEACAM19 Antibody. Lane 1 was treated with the blocking peptide.
DF9343 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
DF9342 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
DF9341 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
Western blot analysis of CPO using COS7 whole cell lysates
DF9339 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
DF9338 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
DF9337 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 extracts from Hepg2, using CPA4 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of CA11 using COS7 whole cell lysates
Western blot analysis of CA10 using HuvEc whole cell lysates
Western blot analysis of CA8 using K562 whole cell lysates
Western blot analysis of extracts from mouse brain, using CA7 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from rat muscle and rat brain, using CHST14 Antibody.
Western blot analysis of CHST5 using COLO205 whole cell lysates
Western blot analysis of CHST3 using Jurkat whole cell lysates
DF9328 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
Western blot analysis of extracts from rat spleen, using CHST11 Antibody.
Western blot analysis of extracts from rat spleen, using CTAG2 Antibody.
Western blot analysis of ARPP19 using NIH-3T3 whole cell lysates

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