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. 2016 Mar 9;7:641–647. doi: 10.1016/j.dib.2016.02.085

Fig. 2.

Fig. 2.

Endogenous immunofluorescence of LC3 and p62 after EBSS ± Baf. A1 treatment in four cell models. Cells were treated with EBSS, Baf. A1 and dual treatment for 4 h, as described in Section 2. Representative images from MEFs (A), HFs (C), SH-SY5Y (E) and N27 cells (G) are shown. Scale bars equate to 10 µm. Histograms show quantification of fluorescence intensity per cell from MEFs (B), HFs (D), SH-SY5Y (F) and N27 cells (H). Data represent the mean±SEM; n=3 (*p≤0.05, **p≤0.01, related to the corresponding non-treated condition).