Brains from representative mice in each group (N = 2–3 per group) were post-fixed overnight followed by paraffin embedding. 5 μm thick sections from cortex were immuno-stained with MAP2 (catalog# AB5622; Millipore, Darmstadt, Germany; 1:500), GFAP (catalog# ab7260; Abcam, 1:5000), and Gli1 (sc-20687; Santacruz, 1:100) and processed as described previously13 (link). ImageJ software was used to quantify IHC data in Fig. 3 and 4 as described previously13 (link).
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