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. 2016 Nov 18;16(1):59–72. doi: 10.1080/15384101.2016.1252881

Figure 5.

Figure 5.

A: PPARγ and glycogen IF in cells treated with scrambled sequence (Scr) and in PPARγ silenced cells (siRNA). Bar = 35 μm. B: WB and densitometric analysis for PPARγ and PYGP. The relative densities of the immunoreactive bands were determined and normalized with respect to GAPDH using a semiquantitative densitometric analysis. Data are mean ± SE of 4 different experiments. *P ≤ 0.05; **P ≤ 0.005. C: Phase contrast microscopy of cells treated with scrambled sequence (Src) and PPARγ silenced cells (siRNA); Bar = 20 μm. D: WB and densitometric analysis for NF-H, PPARβ/δ and PPARα. The relative densities of the immunoreactive bands were determined and normalized with respect to GAPDH using a semiquantitative densitometric analysis. Data are mean ± SE of 4 different experiments. **P ≤ 0.005.