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. Author manuscript; available in PMC: 2014 May 1.
Published in final edited form as: Arterioscler Thromb Vasc Biol. 2013 Feb 21;33(5):999–1005. doi: 10.1161/ATVBAHA.112.300966

Fig. 2. GIT1 protein expression was highly regulated in vivo and in vitro.

Fig. 2

A–D. Immunostaining of GIT1 in carotid arteries of WT and KO mice 14 days after sham or ligation. GIT1 is highly expressed in the intima. Bar=20μm. E. Immunoblot of GIT1 expression in carotid arteries in GIT1 WT and KO mice 7 days after ligation. F. Quantification of GIT1 relative expression normalized to tubulin (Sham = 1.0). *p< 0.05 compared with sham group (mean ±SE; n =3). G. RASM were cultured in serum-free medium for 24h, then treated with and without AngII (10−7 m/L), PDGF (10ng/ml) and 10% FBS for 24h. GIT1 expression was detected by western blot. H. Quantification of GIT1 relative expression normalized to GAPDH (control = 1.0). *p< 0.05 compared with control group (mean ±SE; n =3).