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. Author manuscript; available in PMC: 2014 Oct 16.
Published in final edited form as: Neuroscience. 2013 Jul 1;0:594–601. doi: 10.1016/j.neuroscience.2013.06.044

Fig. 7.

Fig. 7

RNA in situ hybridization analysis of Wnts and their receptor gene expression in mouse embryonic (E11.5) and postanal (P3) spinal cord and DRG. A–N: E11.5 and P3 spinal cord sections were subjected to ISH with Wnt1, Wnt3a, Wint4, Wnt5a, Wnt7a, Wnt7b and Wnt8b riboprobes. O–V: E11.5 and P3 spinal cord sections were subjected to ISH with FZD3, FZD7, FZD8 and FZD10 riboprobes. W–Z: Spinal cord sections from E11.5 embryos were subjected to ISH double labeling with digoxigenin-labeled Wnt7b, FZD7, FZD8 or FZD10 riboprobe (in blue) and fluorescein-labeled sFRP3 riboprobe (in red). The ISH positive cells are indicated by arrows, DRG is outlined by black dashed lines. Scale bar = 100 μm.