Western blot analysis of extracts of various cell lines, using Anti-POLD1 Antibody (A14670) at 1:1,000 dilution. 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.
Immunofluorescence analysis of U2OS cells using Anti-POLD1 Antibody (A14670). Green:gamma H2AX (phospho S139) used for DNA damage marker. DAPI was used to stain the cell nuclei (blue). Cells were treated by UV-A laser.
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