Antibodies

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Western blot analysis of HOXC12 using MCF7 whole cell lysates
Western blot analysis of HOXC11 using MCF7 whole cell lysates
Western blot analysis of HOXC10 using Jurkat whole cell lysates
Western blot analysis of HOXB8 using LOVO whole cell lysates
Western blot analysis of extracts from hybridoma cells, using HOXB3 Antibody. Lane 1 was treated with the blocking peptide.
DF9576 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
DF9575 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
Western blot analysis of HLA-DQB2 using HuvEc whole cell lysates
Western blot analysis of HLA-DMB using Jurkat whole cell lysates
DF9572 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
DF9571 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 extracts from various samples, using HGFAC Antibody.
 Lane 1: hybridoma cells treated with blocking peptide.
 Lane 2: hybridoma cells;
 Lane 3: 293;
Western blot analysis of extracts from mouse brain, using HEATR1 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis GBP5 using COLO205 whole cell lysates
Western blot analysis GUCA2B using K562 whole cell lysates
Western blot analysis GNL3 using LOVO whole cell lysates
Western blot analysis GNB3 using A549 whole cell lysates
Western blot analysis GNB1 using HeLa whole cell lysates
Western blot analysis of extracts from mouse brain, using GNG8 Antibody. Lane 1 was treated with the blocking peptide.
DF9562 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
Western blot analysis GNG5 using HeLa whole cell lysates
Western blot analysis GNG4 using HuvEc whole cell lysates
Western blot analysis of extracts from rat brain, using GNG3 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis GNG2 using Jurkat whole cell lysates

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