BDKRB2抗体 [HL5131]

Untreated (–) and treated (+) unboiled ME-180 whole cell extracts (50 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with BDKRB2 antibody [HL5131] (GTX645327) 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 femto Western HRP Substrate.

Unboiled various whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with BDKRB2 antibody [HL5131] (GTX645327) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data are based on Human Protein Atlas program.

Non-transfected (–) and transfected (+) unboiled 293T whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with BDKRB2 antibody [HL5131] (GTX645327) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.