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

Figure 2.

Figure 2.

Glycogen immunolocalization in SH-SY5Y during differentiation (A). Undifferentiated (CTR) and differentianted (N2) cells at 4h and 24h from N2 treatment. Bar = 70 μm. B: Glycogen IF quantification expressed as Signal Intensity/Unit Surface Area (B). C: WB and relative densitometric analyses for GSK3β in undifferentiated (CTR) and differentiating (N2) cells at the indicated time-points. D: WB and relative densitometric analyses for pGSK3β(Y216) in undifferentiated (CTR) and differentiating (N2) cells at the indicated time-points. E: WB and relative densitometric analyses for pGS(Ser641) in undifferentiated (CTR) and differentiating (N2) cells at the indicated time-points. F: WB and relative densitometric analyses for GS1 and PYGB in undifferentiated (CTR) and differentiating (N2) cells at the indicated time-points. 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 and **P ≤ 0.005.