Protein abundance of EGFR, Ras, and c-Fos in A431
cells. A431 cells were lysed with BlastR lysis
buffer. Sample lysate, as well as EGFR, Ras, and c-Fos recombinant proteins
were separated by SDS-PAGE. Samples were analyzed by western blot using
EGFR, Ras, and c-Fos antibodies. Densitometic analysis of recombinant EGFR
protein was used to establish a standard curve, and concentration of EGFR in
A431 cells was determined based on normalization to that standard curve. Ras
and c-Fos concentrations were determined using the same method with their
respective standard curves.