Antibodies

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DF9427 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
DF9426 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
DF9425 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 of CST5 using NIH-3T3 whole cell lysates
Western blot analysis of CST9L2 using COS7 whole cell lysates
Western blot analysis of CST8 using Jurkat whole cell lysates
Western blot analysis of CTH using HuvEc whole cell lysates
Western blot analysis of CNGB3 using A549 whole cell lysates
Western blot analysis of CNGA3 using COLO205 whole cell lysates
Western blot analysis of HSD11B2 using COLO205 whole cell lysates
Western blot analysis of extracts from Mouse brain, using CNTNAP4 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from HUVEC, using CNTNAP3 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of CNTNAP1 using COS7 whole cell lysates
Western blot analysis of CNTN3 using COLO205 whole cell lysates
Western blot analysis NCAPD3 using LOVO whole cell lysates
Western blot analysis of CR1 using RAW264.7 whole cell lysates
Western blot analysis of CFD using K562 whole cell lysates
DF9410 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 C1QL4 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from various samples, using C1QL3 Antibody.
 Lane 1: 293 treated with blocking peptide.
 Lane 2: 293;
 Lane 3: Hela;
Western blot analysis of HOXD13 using COLO205 whole cell lysates
Western blot analysis of HOXD11 using MCF7 whole cell lysates
Western blot analysis of HOXC9 using COLO205 whole cell lysates
Western blot analysis of extracts from hybridoma cells, using HOXC13 Antibody. Lane 1 was treated with the blocking peptide.

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