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. 2012 Nov 19;7(11):e49862. doi: 10.1371/journal.pone.0049862

Figure 6. Compensatory change in protein expression of other Ca2+ shuttling pathways in mdx muscles.

Figure 6

(A) Absence of the 427 kDa dystrophin in mdx muscles was confirmed and expression levels of STIM1 and SERCA1 in FDB muscles from the wt C57BL/10ScSnJ and dystrophic C57BL/10ScSn-Dmdmdx/J mice were tested by western blot. Sarcomeric a-actin was used as a loading control. (B) In a separate study, the levels of TRPC3/6 and NCX3 were tested in wt and mdx muscles. (C) Densitometry of detected protein expression relative to α-actin, n = 2 for STIM1 and SERCA1 and n = 3 for TrpC3/C6 and NCX, *P<0.10.