Fig. 7.
Stat1 phosphorylation is augmented in IFNγ-stimulated
Fancc−/− macrophages.Peritoneal macrophages from control andFancc−/− mice were stimulated with IFNγ and their cell lysates subjected to Stat1 immunoblotting analysis. (A) Representative filter showing phospho-Stat1 (top panel) and total Stat1 protein (bottom panel). (B) Densitometry analyses of 4 independent experiments demonstrated a significant increase in the phospho-Stat1 signal within Fancc−/− macrophages at 15 minutes after stimulation with IFNγ. *P < .05.