Antibodies

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Western blot analysis of ABCD2 using HeLa whole cell lysates
Western blot analysis of ABCB8 using HeLa whole cell lysates
Western blot analysis of ABCA9 using Jurkat whole cell lysates
Western blot analysis of ABCA7 using Jurkat whole cell lysates
Western blot analysis of ABCA5 using HeLa whole cell lysates
DF9245 at 1/100 staining Mouse brain 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 ABCA12 using LOVO whole cell lysates
Western blot analysis of ABCA10 using Jurkat whole cell lysates
Western blot analysis of extracts from Mouse brain, using ATP5O Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of ATP5L using COLO205 whole cell lysates
Western blot analysis of MT-ATP8 using Jurkat whole cell lysates
DF9239 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
DF9238 at 1/100 staining Human breast 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 C1QTNF9B using Jurkat whole cell lysates
DF9406 at 1/100 staining Mouse 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
DF9405 at 1/100 staining Mouse muscle 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
DF9404 at 1/100 staining Mouse heart 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 CCDC109A Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of COPG using HeLa whole cell lysates
Western blot analysis F13B using COS7 whole cell lysates
Western blot analysis F11 using Jurkat whole cell lysates
Western blot analysis of extracts from mouse brain, using DENND4A Antibody.
Western blot analysis of CLASP2 using COS7 whole cell lysates
Western blot analysis of extracts from B16F10, using CPSF6 Antibody. The lane on the left was treated with blocking peptide.

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