Antibodies

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Western blot analysis of Cytochrome P450 46A1 using HuvEc whole cell lysates
DF8925 staining HuvEc 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 Cytochrome c Oxidase 8C using Jurkat whole cell lysates
DF8923 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
DF8922 at 1/100 staining Rat heart 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 Cytochrome c Oxidase 3 using Jurkat whole cell lysates
Western blot analysis of extracts from various samples, using Cytochrome c Oxidase 1 Antibody.
 Lane 1: 3T3, treated with blocking peptide;
 Lane 2: 3T3;
 Lane 3: Myeloma cells.

Observed bands: 73 kDa.
DF8919 at 1/100 staining Rat colon 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
DF8918 at 1/100 staining Rat 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
DF8917 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
Western blot analysis of CDCA7L using MCF7 whole cell lysates
Western blot analysis of CDK5RAP1 using HuvEc whole cell lysates
Western blot analysis of CISH using Jurkat whole cell lysates
Western blot analysis of CIDEC using HeLa whole cell lysates
Western blot analysis of CELSR2 using MCF7 whole cell lysates
Western blot analysis of CDK3 using HuvEc whole cell lysates
Western blot analysis of CD320 using HuvEc whole cell lysates
Western blot analysis of Cytochrome P450 2F1 using Jurkat whole cell lysates
DF8908 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 COX15 using HT29 whole cell lysates
Western blot analysis of Collagen XVI ?1 using K562 whole cell lysates
Western blot analysis of extracts from hela, using Collagen IX ?2 Antibody. Lane 1 was treated with the blocking peptide.
DF8904 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 of Collagen VIII ?2 using LOVO whole cell lysates

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