Fig. 4From: Effects of platelet-rich plasma on the activity of human menstrual blood-derived stromal cells in vitroQuantitative RT-PCR analysis of receptivity- and inflammation-related genes. Gene expression analyzed by RT-PCR. P4 MenSCs (n = 6) cultured with 10% PRP (gray) or 10% FBS (white) for 6 h and 24 h. RT-PCR analysis of FoxO1, HOXA10, LIF, CK18, IL1-β, IL6, RUNX2, and PPARγ2. GAPDH was used for mRNA standard, fold changes were measured by 2-ΔΔCT. Data was mean ± SEM, *P < 0.05, **P < 0.01, ***P < 0.001 for two-tailed t testBack to article page