Antibodies

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Western blot analysis GINS2 using Jurkat whole cell lysates
Western blot analysis GINS1 using HT29 whole cell lysates
Western blot analysis of extracts from HepG2, using POLG1 Antibody. The lane on the left was treated with blocking peptide.
DF9448 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
DF9447 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 of POLE2 using LOVO whole cell lysates
Western blot analysis of APOBEC3H using A549 whole cell lysates
Western blot analysis of DCLRE1B using COLO205 whole cell lysates
Western blot analysis of extracts from rat muscle, using DLG3 Antibody.
Western blot analysis of DGAT2 using K562 whole cell lysates
Western blot analysis of ASAP2 using LOVO whole cell lysates
Western blot analysis of DSG4 using HeLa whole cell lysates
Western blot analysis of DSG3 using LOVO whole cell lysates
DF9438 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 DHRS7 using Jurkat whole cell lysates
Western blot analysis of DHRS11 using Jurkat whole cell lysates
Western blot analysis of DHRS10 using K562 whole cell lysates
Western blot analysis of extracts from rat brain, using DHRS1 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of extracts from rat muscle, using DOCK7 Antibody.
Western blot analysis of DOCK11 using K562 whole cell lysates
DF9431 at 1/100 staining Human prostate 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 PLA2G4F Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of PLA2G4B using K562 whole cell lysates
Western blot analysis of CNDP2 using K562 whole cell lysates

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