“…The following pairs of double immunofluorescence were carried out: (1) srGAP1 and neurofilament 200, (2) srGAP3 and S100, (3) srGAP3 and glial fibrillary acidic protein (GFAP), (4) srGAP3 and NF200, and (5) srGAP3 and Robo2. Final dilutions of these primary antibodies were: mouse anti‐srGAP1 (1:300) (Abcam, Hong Kong), rabbit anti‐srGAP3 (1:400) (Abcam, Hong Kong), rat anti‐srGAP3 (Abcam, Hong Kong), mouse anti‐GFAP (1:400) (Millipore USA), chicken anti‐GFAP (1:400) (Millipore), rat anti‐NF200 (1:400; Sigma), mouse anti‐Robo2 (1:400) (Abcam, Hong Kong), rabbit anti‐srGAP3 (1:400), and mouse anti‐S100 (1:400) (Millipore) antibodies (Zheng et al,2008,2010). Secondary antibodies included fluorescein isothiocyanate (FITC)‐goat anti‐mouse IgG (1:200), FITC‐goat anti‐chicken IgG (1:200), Cy3‐goat anti‐rabbit IgG (1:200) (Boster, China), FITC‐goat anti‐rat IgG (1:200) (Boster, China).…”