Untreated (–) and treated (+) HeLa whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PARP antibody [GT1176] (GTX09509) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PARP antibody [GT1176] (GTX09509) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.

IHC-P analysis of mouse spleen tissue section using GTX09509 PARP antibody [GT1176].
Dlution : 1:100

IHC-P analysis of rat spleen tissue section using GTX09509 PARP antibody [GT1176].
Dlution : 1:100

WB analysis of Wild-type (WT) and PARP knockout (KO) HeLa cell extracts using GTX09509 PARP antibody [GT1176].
Dilution : 1:1000
Loading : 25μg

WB analysis of Jurkat cells were treated with/without Staurosporine (1μM) at RT for 3 hrs using GTX09509 PARP antibody [GT1176].
Dilution : 1:1000
Loading : 25μg

IHC-P analysis of hmuan appendix tissue section using GTX09509 PARP antibody [GT1176].
Dlution : 1:100