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. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: DNA Repair (Amst). 2018 May 18;68:1–11. doi: 10.1016/j.dnarep.2018.05.003

Fig. 1.

Fig. 1.

Normal fibroblast cell (GM00637) and Werner syndrome fibroblast cell (AG11395) were treated with ER stress inducer tunicamycin. Control cells were incubated with complete medium. (A) Graphical representation of MDC staining at different time points 2–24 h of all the cells. More than 600 cells were analysed for each condition. (B) Immunobloting of total cellular extract for autophagy marker proteins of normal fibroblast GM00637 and WS cell AG11395. (C) Graphical representation of ratio LC3BII and LC3BI of both cell lines. (D) Graphical representation of ratio Beclin-1 and Actin of both cell lines. (E) Graphical representation of ratio Atg5 and Actin of both cell lines. 3 western blots from 3 separate sets of experiments were used.