Fig. 6
From: Methionine sulfoxide reductase B2 protects against cardiac complications in diabetes mellitus

ROS induced methionine sulfoxidation (MetO) in human diabetic hearts. A. Western blot analysis of MetO in normal (NH #1–3) and diabetic human heart tissue(DH #1–6). GAPDH served as a loading control. B. Quantification of MetO signal intensity. C. Western blot analysis of methionine sulfoxide reductase A and B2 (MsrA and B2) in normal (NH #1–3) and diabetic heart tissue (DH #1–6). GAPDH served as loading a loading control. D. Quantification of MsrA and MsrB2 signal intensity. E. Western blot analysis of LC3l/II and p62 in normal (NH #1–3) and diabetic heart tissue (DH #1–6). GAPDH served as a loading control. F. Quantification of LC3l/II and p62 signal intensity. G. Western blot analysis of DRP1 and OPA1 in normal (NH #1–3) and diabetic heart tissues (DH #1–6). GAPDH served as a loading control. H. Quantification of MetO intensity