Research Paper Volume 13, Issue 10 pp 13926—13940

Peroxiredoxin II with dermal mesenchymal stem cells accelerates wound healing

Characterization of DMSCs. (A) DMSCs were analyzed by FACS after staining with FITC- or PE-conjugated control isotype IgG (black peaks) or antibodies against the indicated cell-surface proteins. (B) DMSC differentiation. DMSCs were cultured in appropriate differentiation media to promote differentiation into adipocytes, as indicated by oil red O staining, and (C) osteoblasts, as indicated by alizarin red staining.

Figure 1. Characterization of DMSCs. (A) DMSCs were analyzed by FACS after staining with FITC- or PE-conjugated control isotype IgG (black peaks) or antibodies against the indicated cell-surface proteins. (B) DMSC differentiation. DMSCs were cultured in appropriate differentiation media to promote differentiation into adipocytes, as indicated by oil red O staining, and (C) osteoblasts, as indicated by alizarin red staining.