Western Blot - Anti-ATR (phospho Ser428) Antibody (A91791)
Western blot analysis of 293T, using Anti-ATR (phospho Ser428) Antibody (A91791) at 1:400 dilution. 293T cells were treated by UV at room temperature for 15-30 minutes. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 90s.
Western Blot - Anti-ATR (phospho Ser428) Antibody (A91791)
Western blot analysis of NIH/3T3, using Anti-ATR (phospho Ser428) Antibody (A91791) at 1:400 dilution. NIH/3T3 cells were treated by Nocodazole (50 ng/ml) at 37°C for 20 hours. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 90s.
Immunohistochemistry analysis of paraffin-embedded human testis using Anti-ATR (phospho Ser428) Antibody (A91791) at a dilution of 1:100 (40x lens). Perform high pressure antigen retrieval with 10 mM citrate buffer pH 6.0 before commencing with IHC staining protocol.
Immunohistochemistry analysis of paraffin-embedded mouse testis using Anti-ATR (phospho Ser428) Antibody (A91791) at a dilution of 1:100 (40x lens). Perform high pressure antigen retrieval with 10 mM citrate buffer pH 6.0 before commencing with IHC staining protocol.
Immunohistochemistry analysis of paraffin-embedded rat testis using Anti-ATR (phospho Ser428) Antibody (A91791) at a dilution of 1:100 (40x lens). Perform high pressure antigen retrieval with 10 mM citrate buffer pH 6.0 before commencing with IHC staining protocol.
Immunofluorescence analysis of U2OS cells using Anti-ATR (phospho Ser428) Antibody (A91791) at a dilution of 1:100. DAPI was used to stain the cell nuclei (blue).