Antibodies

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DF8951 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 FGFBP3 using HT29 whole cell lysates
Western blot analysis of extracts from mouse liver, using FGF6 Antibody.
Western blot analysis FGF4 using RAW264.7 whole cell lysates
Western blot analysis FGF21 using COLO205 whole cell lysates
Western blot analysis of extracts from mouse brain, using FGF20 Antibody.
DF8945 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
DF8944 at 1/100 staining Human Melanoma 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 FAT1 using Jurkat whole cell lysates
Western blot analysis of HJURP using COLO205 whole cell lysates
DF8941 at 1/100 staining Mouse 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
DF8940 at 1/100 staining Mouse 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
DF8939 at 1/100 staining Human liver 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
Western blot analysis of Cytochrome b561 using RAW264.7 whole cell lysates
Western blot analysis of Cytochrome c Oxidase 7B2 using RAW264.7 whole cell lysates
Western blot analysis of Cytochrome c Oxidase 7A2 using A549 whole cell lysates
Western blot analysis of Cytochrome c Oxidase 6B1 using COLO205 whole cell lysates
Western blot analysis of extracts from Rat heart, using Cytochrome c Oxidase 6A1 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of HspB4 using A549 whole cell lysates
Western blot analysis of CRY1 using A549 whole cell lysates
Western blot analysis of extracts from Rat heart, using CRLF3 Antibody. The lane on the left was treated with blocking peptide.
DF8930 at 1/100 staining Human lung 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
Western blot analysis of extracts from various samples, using Cytochrome P450 4F22 Antibody.
 Lane 1: Hela treated with blocking peptide;
 Lane 2: Hela;
 Lane 3: HepG2.
Western blot analysis of Cytochrome P450 4F8 using Jurkat whole cell lysates

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