Double in situ hybridization was carried out by using fluorescein/fast red detection for TrkA (A, E), TrkB (B, F), TrkC (C, G), c-ret (D, H) and DIG/NBT-BCIP for Dok4 (A, B, C, D) and Crip2 (E, F, G, H)
<p><b>Copyright information:</b></p><p>Taken from "A SAGE-based screen for genes expressed in sub-populations of neurons in the mouse dorsal root ganglion"</p><p>http://www.biomedcentral.com/1471-2202/8/97</p><p>BMC Neuroscience 2007;8():97-97.</p><p>Published online 19 Nov 2007</p><p>PMCID:PMC2241628.</p><p></p> In situ signals were converted into pseudo colors and images were superimposed to show co-labelling of cells. Dok4 co-localised with all major subtypes of DRG neurons, Crip2 was specifically excluded from TrkC population. Scale bar 50 μm
