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. Author manuscript; available in PMC: 2013 Dec 15.
Published in final edited form as: Dev Biol. 2012 Sep 27;372(2):217–228. doi: 10.1016/j.ydbio.2012.09.015

Figure 6. CR2-GFP+ cells are asymmetrically dividing interneuron precursors in P0 transgenic mouse.

Figure 6

Fluorescent microphotographs of coronal (A) and sagittal (B,C) brain sections of the transgenic mouse at P0. CR2-GFP+ cells co-stained with cell specific markers. (D) Histograph represents the percentage of CR2-GFP+ cells co-stained with radial glial markers Notch1 (4±3%) and BLBP (9±5%) (A); an asymmetric division marker NuMa (47±21%) and a marker for GABAergic interneuron progenitor GAD65/67 (59±14%) (B); and an early neuronal marker DCX (14±2%), a layer VI neuronal marker Tbr1 (6±4%), and an astrocyte marker GFAP (5±9%) (C). Scale bar = 20 μm.