beta Catenin (phospho Ser33) antibody [HL5105]

Untreated (–) and treated (+) PC-12 whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with beta Catenin (phospho Ser33) antibody [HL5105] (GTX645299) diluted at 1:500 and beta Catenin antibody [HL1753] (GTX637403) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Untreated (–) and treated (+) PC-3 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membranes were blotted with beta Catenin (phospho Ser33) antibody [HL5105] (GTX645299) diluted at 1:1000 and beta Catenin antibody [HL1753] (GTX637403) diluted at 1:1000. 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.

Untreated (–) and treated (+) NIH-3T3 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membranes were blotted with beta Catenin (phospho Ser33) antibody [HL5105] (GTX645299) diluted at 1:1000 and beta Catenin antibody [HL1753] (GTX637403) diluted at 1:1000. 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.