Antibodies

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Western blot analysis of extracts from Rat liver, using CALR3 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis NTHL1 using RAW264.7 whole cell lysates
Western blot analysis of extracts from rat muscle, using ENDOD1 Antibody.
Western blot analysis of ELP3 using HuvEc whole cell lysates
Western blot analysis of ELOVL2 using COLO205 whole cell lysates
Western blot analysis GFM1 using Jurkat whole cell lysates
Western blot analysis of extracts from rat muscle, using EEF1A2 Antibody.
DF9492 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
DF9491 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
Western blot analysis of RNF5 using Jurkat whole cell lysates
Western blot analysis of extracts from mouse brain, using RNF167 Antibody.
DF9488 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
DF9487 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
DF9486 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 MARCH9 using MCF7 whole cell lysates
Western blot analysis of MARCH8 using HuvEc whole cell lysates
Western blot analysis of MARCH7 using HuvEc whole cell lysates
Western blot analysis of MARCH6 using Jurkat whole cell lysates
Western blot analysis of extracts from rat muscle, mouse brain, using MARCH1 Antibody.
Western blot analysis of extracts from rat muscle, using LRSAM1 Antibody.
Western blot analysis of HECW1 using K562 whole cell lysates
Western blot analysis of extracts from rat brain, using HECTD1 Antibody.
DF9477 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 FANCL using LOVO whole cell lysates

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