Antibodies

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Western blot analysis of MED9 using Jurkat whole cell lysates
Western blot analysis of MED4 using HT29 whole cell lysates
Western blot analysis of MED31 using MCF7 whole cell lysates
Western blot analysis of extracts from Rat liver, using MED30 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of extracts from Mouse brain, using MED29 Antibody. The lane on the left was treated with blocking peptide.
DF9615 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
DF9614 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
DF9613 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 Hela, using MED11 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of MARVELD2 using HepG2 whole cell lysates
Western blot analysis of extracts from 3t3, using LRP4 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of LRP1B using NIH-3T3 whole cell lysates
Western blot analysis of LRP12 using Jurkat whole cell lysates
Western blot analysis of ACSL5 using 293 whole cell lysates
Western blot analysis of ACSL3 using Jurkat whole cell lysates
Western blot analysis of extracts from mouse muscle, using ACSL1 Antibody. Lane 1 was treated with the blocking peptide.
DF9604 at 1/100 staining Human lymph node 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 LILRB1 using K562 whole cell lysates
Western blot analysis of A4GALT using K562 whole cell lysates
Western blot analysis of KIR2DS5 using LOVO whole cell lysates
Western blot analysis of KIR2DL5A using K562 whole cell lysates
Western blot analysis of KIR2DL2 using NIH-3T3 whole cell lysates
Western blot analysis of KHDRBS3 using Jurkat whole cell lysates
DF9597 at 1/100 staining Human Head and neck 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

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