Antibodies

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Western blot analysis of Collagen VIII ?1 using LOVO whole cell lysates
Western blot analysis of Collagen VII ?1 using HeLa whole cell lysates
DF8900 at 1/100 staining human brain tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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 ZHX2 using Jurkat whole cell lysates
DF8898 staining Hela 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 SOX21 using HepG2 whole cell lysates
Western blot analysis NCOR2 using NIH-3T3 whole cell lysates
DF8895 at 1/100 staining Mouse liver 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 WNK2 using Jurkat whole cell lysates
Western blot analysis of THRAP3 using HeLa whole cell lysates
Western blot analysis STRN4 using mouse brain lysates
DF9064 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
DF9063 at 1/100 staining Rat brain 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
DF9062 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
Western blot analysis of CENPQ using Jurkat whole cell lysates
Western blot analysis of CENPP using K562 whole cell lysates
Western blot analysis of CENPK using COLO205 whole cell lysates
Western blot analysis of CENPH using COLO205 whole cell lysates
Western blot analysis of CENPC1 using Jurkat whole cell lysates
Western blot analysis of EDA-A1 Receptor using Jurkat whole cell lysates
Western blot analysis of RAD54B using COLO205 whole cell lysates
Western blot analysis GZMA using COLO205 whole cell lysates
DF9053 at 1/100 staining Human 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 LAMC2 using HepG2 whole cell lysates

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