Antibodies

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Western blot analysis of MMP21 using COS7 whole  lysates.
Western blot analysis of MMP20 using Jurkat whole  lysates.
Western blot analysis of ABCG1 using HT29 whole  lysates.
Western blot analysis of STK3 using COS7 whole  lysates.
DF7691 at 1/100 staining human Lymph node 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 IPO9 using COLO205 whole  lysates.
Western blot analysis of extracts from Hela, using TGIF1 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from rat brain,mouse brain, using IHH Antibody.
Western blot analysis of SUFU using HuvEc whole  lysates.
Western blot analysis of MMP12 using Jurkat whole  lysates.
Western blot analysis of DNAJC3 using HuvEc whole  lysates.
Western blot analysis of TIRAP using K562 whole  lysates.
DF7683 staining HEPG2 cells by ICC/IF. Cells were fixed with PFA and permeabilized in 0.1% saponin prior to blocking in 10% serum for 45 minutes at 37¡ãC. The primary antibody was diluted 1/200 and incubated with the sample for 1 hour at 37¡ãC. A  Alexa Fluor 594 conjugated goat polyclonal to rabbit IgG (H+L), diluted 1/600 was used as secondary antibod
DF7682 staining HepG2 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 EPS15L1 using HeLa whole  lysates.
DF7680 staining HepG2 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
DF7678 staining HepG2 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 ACTC1 using Jurkat whole  lysates.
DF7676 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 KCND2 using MCF7 whole  lysates.
DF7674 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 NEFM using 293 whole  lysates.
Western blot analysis of CHGA using LOVO whole  lysates.
Western blot analysis of CNN1 using NIH-3T3 whole  lysates.

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