Research Article

Proteomic Profiling of the Dystrophin-Deficient MDX Heart Reveals Drastically Altered Levels of Key Metabolic and Contractile Proteins

Figure 6

Graphical presentation of the immunoblot analysis of cardiac marker proteins in dystrophic tissue. Shown is the graphical presentation of the statistical evaluation of immuno-decoration using antibodies to adenylate kinase isoform AK1 (a), fatty acid binding protein FABP3 (b), isocitrate dehydrogenase ICDH (c), porin isoform VDAC1 (d), ATP synthase (e), desmin (f), slow/cardiac myosin heavy chain MHCs (G) and succinate dehydrogenase SDH (H). The comparative blotting was statistically evaluated using an unpaired Studentโ€™s t-test ( ๐‘› = 5 ; โˆ— ๐‘ƒ < . 0 5 ; โˆ— โˆ— ๐‘ƒ < . 0 1 ). The concentration of desmin, myosin heavy chain and succinate dehydrogenase was found not to be significantly different between normal and dystrophic preparations. Lanes 1 and 2 represent normal and dystrophic muscle extracts from control and MDX mice, respectively.
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