Antibodies

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Western blot analysis IFRD2 using HuvEc whole cell lysates
Western blot analysis IFNK using HuvEc whole cell lysates
Western blot analysis IFNA8 using K562 whole cell lysates
Western blot analysis IFNA7 using HepG2 whole cell lysates
Western blot analysis IFNA6 using HeLa whole cell lysates
DF8970 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 IFN21 using Jurkat whole cell lysates
Western blot analysis of extracts from Hela, using IFN17 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis IFN16 using K562 whole cell lysates
Western blot analysis IFN14 using HeLa whole cell lysates
Western blot analysis of extracts from Hela, using IFN10 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis IFM2 using Jurkat whole cell lysates
Western blot analysis IFIT3 using Jurkat whole cell lysates
DF8962 at 1/100 staining Human cervical 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
DF8961 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
DF8960 at 1/100 staining Human 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
Western blot analysis IBP6 using Jurkat whole cell lysates
Western blot analysis of extracts from 293, using IBP4 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis IL10RB using COLO205 whole cell lysates
Western blot analysis of HSP76 using Jurkat whole cell lysates
Western blot analysis of HSP74 using HepG2 whole cell lysates
Western blot analysis of HSBP1 using HT29 whole cell lysates
Western blot analysis GTSE1 using LOVO whole cell lysates
Western blot analysis GPD1 using COLO205 whole cell lysates

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