Western blot analysis of extracts of HepG2 cells, using Phospho-PDGFR alpha-Y1018 antibody at 1:1000 dilution. HepG2 cells were treated by UV for 15-30 minutes or treated by EGF for 30 minutes after serum-starvation overnight.
Secondary antibody: HRP Goat Anti-Rabbit IgG at 1:10000 dilution.
Lysates/proteins: 25ug per lane.
Blocking buffer: 3% BSA.
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