Figure 4
(A–D) Western blot analysis of Sirt3, Idh2, and FOXO3a levels in BMSCs. Acetylated Idh2 and FOXO3a were isolated by immunoprecipitation with anti-Idh2 and anti-FOXO3a antibody followed by Western blotting with anti-acetyl-lysine antibody (n=3). (E) Detection of Sirt3 relative activity in BMSCs (n=3), significant differences (P<0.05) were observed among a–c. (F,G) Detection of Idh2 and FOXO3a acetylation level in BMSCs, significant differences (P<0.05) were observed among a–c. All the experiments were repeated at least thrice (n≥3). Data were presented as means ± SD. P<0.05 by one-way ANOVA with Tukey’s post hoc test (three or more groups).
NMNAT3 enhanced the activity of Sirt3 under oxidative stress

(A–D) Western blot analysis of Sirt3, Idh2, and FOXO3a levels in BMSCs. Acetylated Idh2 and FOXO3a were isolated by immunoprecipitation with anti-Idh2 and anti-FOXO3a antibody followed by Western blotting with anti-acetyl-lysine antibody (n=3). (E) Detection of Sirt3 relative activity in BMSCs (n=3), significant differences (P<0.05) were observed among a–c. (F,G) Detection of Idh2 and FOXO3a acetylation level in BMSCs, significant differences (P<0.05) were observed among a–c. All the experiments were repeated at least thrice (n≥3). Data were presented as means ± SD. P<0.05 by one-way ANOVA with Tukey’s post hoc test (three or more groups).

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