STAT2 (phospho Tyr690)抗体 [HL4208]

Untreated (–) and treated (+) A20 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membranes were blotted with STAT2 (phospho Tyr690) antibody [HL4208] (GTX643031) diluted at 1:1000 and STAT2 antibody [C2C3], C-term (GTX103117) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Untreated (–) and treated (+) A20 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membranes were blotted with STAT2 (phospho Tyr690) antibody [HL4208] (GTX643031) diluted at 1:1000 and highly cited STAT2 antibody [C2C3], C-term (GTX103117) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Untreated (–) and treated (+) HeLa whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membranes were blotted with STAT2 (phospho Tyr690) antibody [HL4208] (GTX643031) diluted at 1:1000 and STAT2 antibody [C2C3] (GTX103117) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Untreated (–) and treated (+) PC-12 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membranes were blotted with STAT2 (phospho Tyr690) antibody [HL4208] (GTX643031) diluted at 1:1000 and STAT2 antibody(GTX103117) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.