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. 2019 Feb 20;23:60–74. doi: 10.1016/j.molmet.2019.02.004

figs3.

figs3

Figure S3. (A) Cell size quantification of adipocytes in rWAT from of 6 weeks old myf5-Cre;R26R-mTmG (grey circles), Akt1myf5cKO;R26R-mTmG (blue squares) and Akt2myf5cKO;R26R-mTmG mice (Akt2 deficient as green triangles and Akt2 wildtype as red circles). The number of adipocytes analyzed are: n = 187 for myf5-Cre;R26R-mTmG, n = 152 for Akt1myf5cKO;R26R-mTmG and n = 219 GFP+ and 82 Tomato+ for Akt2myf5cKO;R26R-mTmG. One-way ANOVA was used for statistical analysis. (B) Percentage (average ± SD) of mTFP+ (Red) and mGFP+ (Green) APCs isolated from the indicated depots from 6 weeks old myf5-Cre; R26R-mTmG, Akt1myf5cKO;R26R-mTmG and Akt2myf5cKO;R26R-mTmG mice (n = 3 for myf5-Cre; R26R-mTmG, 2 for Akt1myf5cKO;R26R-mTmG and 4 for Akt2myf5cKO;R26R-mTmG; no statistical analysis was used). A total of 50000 singles were used for this analysis. (C) Western blot of Akt2myf5cKO and control (Akt2 floxed) rWAT after overnight fasting with or without refeeding. (D) Western blot of Akt1myf5cKO, Akt2myf5cKO and control (Akt1 floxed and Akt2 floxed, respectively) quadriceps after overnight fasting with or without refeeding.