Antibodies

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Western blot analysis of extracts from HepG2, using B4GALT4 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of B4GALT2 using Jurkat whole cell lysates
Western blot analysis of extracts from Myeloma cells, using B4GALNT2 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of B3GALT6 using HuvEc whole cell lysates
Western blot analysis of B3GALT5 using HT29 whole cell lysates
Western blot analysis of extracts from VERO, using B3GALT2 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of extracts from Myeloma cells, using GCNT4 Antibody. The lane on the left was treated with blocking peptide.
BNIPL Antibody on lung cancer by IHC.
Western blot analysis of BATF2 using HeLa whole cell lysates
Western blot analysis of extracts from various samples, using BAGE5 Antibody.
 Lane 1: VERO treated with blocking peptide;
 Lane 2: VERO;
 Lane 3: HepG2.
Western blot analysis of AXIN1 using HT29 whole cell lysates
Western blot analysis of KCNJ8 using Jurkat whole cell lysates
Western blot analysis of KCNJ15 using HeLa whole cell lysates
Western blot analysis of extracts from various samples, using KCNJ14 Antibody.
 Lane 1: Myeloma cells treated with blocking peptide;
 Lane 2: Myeloma cells;
 Lane 3: COS-7;
 Lane 4: Rat  spleen.
Western blot analysis of extracts from HepG2, using KCNJ10 Antibody. Lane 1 was treated with the blocking peptide.
DF9259 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
Western blot analysis of DDX18 using HuvEc whole cell lysates
Western blot analysis of RECQL4 using K562 whole cell lysates
DF9256 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
DF9255 at 1/100 staining Human urothelial 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 extracts from hepg2, using ABCC8 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of ABCC11 using Jurkat whole cell lysates
Western blot analysis of ABCG4 using COLO205 whole cell lysates
Western blot analysis of ABCF3 using K562 whole cell lysates

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