Antibodies

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Western blot analysis NSMCE2 using LOVO whole cell lysates
Western blot analysis of DYNLT3 using HeLa whole cell lysates
Western blot analysis of DYNLT1 using COLO205 whole cell lysates
Western blot analysis of DYNLRB2 using Jurkat whole cell lysates
Western blot analysis of extracts from Mouse Myeloma cell, using DYNLRB1 Antibody. Lane 1 was treated with the blocking peptide.
DF9470 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
DF9469 at 1/100 staining Mouse 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 DCTN4 using COLO205 whole cell lysates
Western blot analysis of RPAB4 using Jurkat whole cell lysates
DF9466 at 1/100 staining Rat 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 RPAB2 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of POLR1D using COLO205 whole cell lysates
Western blot analysis of POLRMT using MCF7 whole cell lysates
Western blot analysis of RPC9 using HuvEc whole cell lysates
Western blot analysis of RPC7 using HuvEc whole cell lysates
Western blot analysis of RPC6 using HeLa whole cell lysates
Western blot analysis of extracts from mouse brain, using RPC10 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from various samples, using RPB7 Antibody.
 Lane 1: Hela treated with blocking peptide.
 Lane 2: Hela;
 Lane 3: HepG2;
DF9457 staining Hela 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) Ab, diluted at 1/600, was used as the secondary antibod
Western blot analysis of TWISTNB using MCF7 whole cell lysates
DF9455 at 1/100 staining Human 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
Western blot analysis of extracts from mouse kidney, using IGHMBP2 Antibody.
Western blot analysis of DNA2L using COLO205 whole cell lysates
Western blot analysis of TOP1MT using COLO205 whole cell lysates

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