Antibodies

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Western blot analysis SHOX using MCF7 whole cell lysates
Western blot analysis of extracts from Rat  spleen, using SH3GL3 Antibody. The lane on the left was treated with blocking peptide.
DF9906 at 1/100 staining Human 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
DF9905 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 extracts from Mouse brain, using SH3BGRL2 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis SH3TC2 using NIH-3T3 whole cell lysates
Western blot analysis SH3PXD2A using NIH-3T3 whole cell lysates
Western blot analysis SHANK3 using Jurkat whole cell lysates
Western blot analysis of extracts from various samples, using STAC3 Antibody.
 Lane 1: 293 treated with blocking peptide.
 Lane 2: 293;
 Lane 3: HUVEC;
Western blot analysis of extracts from various samples, using NCKIPSD Antibody.
 Lane 1: Hela treated with blocking peptide.
 Lane 2: Hela;
 Lane 3: HepG2;
Western blot analysis SH2B3 using MCF7 whole cell lysates
Western blot analysis SH2D4A using K562 whole cell lysates
DF9896 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 SERPINB6 using K562 whole cell lysates
Western blot analysis SERPINB10 using LOVO whole cell lysates
Western blot analysis of PPP4R1 using K562 whole cell lysates
Western blot analysis of VRK1 using NIH-3T3 whole cell lysates
Western blot analysis ULK4 using Jurkat whole cell lysates
DF9890 at 1/100 staining Human 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
DF9889 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
DF9888 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
DF9887 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 NEK4 using HepG2 whole cell lysates
Western blot analysis of extracts from HepG2, using STK38L Antibody.

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