Antibodies

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DF9509 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
DF9508 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 EIF1B using COLO205 whole cell lysates
Western blot analysis of HSD17B8 using A549 whole cell lysates
Western blot analysis of HSD17B12 using A549 whole cell lysates
Western blot analysis of extracts from Hepg2, using EDEM3 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of EDEM2 using COS7 whole cell lysates
Western blot analysis of EDEM1 using NIH-3T3 whole cell lysates
Western blot analysis of EDC4 using Jurkat whole cell lysates
Western blot analysis of CD248 using COLO205 whole cell lysates
DF9499 at 1/100 staining Mouse pancreas 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 NRSN2 using K562 whole cell lysates
DF9680 at 1/100 staining Human gastric 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
DF9679 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 NPHP1 using HepG2 whole cell lysates
Western blot analysis NCR2 using Jurkat whole cell lysates
DF9676 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
DF9675 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
DF9674 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 HepG2 and mouse heart, using CYB5R2 Antibody.
Western blot analysis NDUFS8 using LOVO whole cell lysates
Western blot analysis NDUFS6 using NIH-3T3 whole cell lysates
Western blot analysis NDUFS4 using K562 whole cell lysates
Western blot analysis NDUFS2 using COLO205 whole cell lysates

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