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. Author manuscript; available in PMC: 2016 Sep 20.
Published in final edited form as: Glia. 2011 Jun 8;59(10):1518–1528. doi: 10.1002/glia.21195

Fig. 1.

Fig. 1

Differentiation of neural progenitor cultures. (A) NSCs from striatal tissues of P1 C57/B6 litters were differentiated and subsequently stained with antibodies reactive to either mouse NG2 or O1. (B) After 6 days, both NG2 and O1 cells were detected by immunofluorescent staining. In (A) and (B), nuclei were stained with DAPI (blue). (C) Frequency of NG2+O1 and NG2O1+ cells at days 0 and 6 postdifferentiation. Data represent the percentage of cells staining positive for either antigen and presented as average ± SD from two independent experiments. **Statistical significance for P values ≤0.001. For (A) and (B), scale bar = 40 μm.