Untreated (–) and treated (+) 293T whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.

Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) 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 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.

ICC/IF analysis of NIH-3T3 cells using GTX03239 PER3 antibody [GT1327].
Blue : DAPI for nuclear staining
Dilution : 1:100

WB analysis of various samples using GTX03239 PER3 antibody [GT1327].
Dilution : 1:1000
Loading : 25μg per lane