Antibodies

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Western blot analysis NDUFV1 using K562 whole cell lysates
Western blot analysis of extracts from mouse spleen, using NDUFC1 Antibody.
Western blot analysis NDUFB8 using HuvEc whole cell lysates
DF9665 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 NDUFB5 using COS7 whole cell lysates
Western blot analysis NDUFB3 using LOVO whole cell lysates
Western blot analysis NDUFA7 using K562 whole cell lysates
Western blot analysis NDUFA6 using RAW264.7 whole cell lysates
Western blot analysis NDUFA5 using RAW264.7 whole cell lysates
Western blot analysis NDUFA1 using K562 whole cell lysates
DF9658 at 1/100 staining Human 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
DF9657 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 of extracts from mouse spleen, using MYO16 Antibody.
Western blot analysis of MYO7A using HT29 whole cell lysates
DF9654 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 extracts from Hela, using MYO5C Antibody. Lane 1 was treated with the blocking peptide.
DF9652 at 1/100 staining  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
Western blot analysis of MYO1B using COLO205 whole cell lysates
Western blot analysis of extracts from rat brain, using MYO1A Antibody.
Western blot analysis of MYBPC2 using mouse liver lysates
Western blot analysis of MYH8 using HepG2 whole cell lysates
Western blot analysis of extracts from Hela, using MYH3 Antibody. Lane 1 was treated with the blocking peptide.
DF9646 at 1/100 staining human Prostate carcinoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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 MAL using COLO205 whole cell lysates

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