Antibodies

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Western blot analysis of PDE3B using HuvEc whole cell lysates
Western blot analysis of PDE3A using COS7 whole cell lysates
Western blot analysis of extracts from rat muscle and mouse brain, using PDE2A Antibody.
Western blot analysis of CP using K562 whole cell lysates
DF9368 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 extracts from mouse brain, using CEP250 Antibody.
DF9366 at 1/100 staining Human brain 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
DF9365 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 CEP68 using COLO205 whole cell lysates
Western blot analysis of CEP63 using Jurkat whole cell lysates
DF9362 at 1/100 staining RAT testis 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
DF9361 at 1/100 staining Rat 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
DF9360 at 1/100 staining Mouse 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
Western blot analysis of ACAP2 using K562 whole cell lysates
Western blot analysis of CRABP1 using COLO205 whole cell lysates
Western blot analysis of CGRRF1 using K562 whole cell lysates
Western blot analysis of BORG5 using mouse liver lysates
Western blot analysis of extracts from various samples, using SLC7A3 Antibody.
 Lane 1: HepG2 treated with blocking peptide.
 Lane 2: HepG2;
 Lane 3: mouse brain;
Western blot analysis of M6PR using mouse brain lysates
Western blot analysis of CHAC1 using Jurkat whole cell lysates
Western blot analysis of CATSPERB using COLO205 whole cell lysates
DF9351 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 CATSPER3 using Jurkat whole cell lysates
Western blot analysis of CATSPER1 using K562 whole cell lysates

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