Abstract
The cardiac troponin C (cTnC) subunit of the troponin complex is expressed in both slow skeletal and cardiac muscle. Therefore, investigating the effects of cTnC mutations associated with hypertrophic cardiomyopathy (HCM) in slow skeletal muscle may reveal new insights into the mechanisms underlying cardiomyopathies. Glycerol SDS-PAGE analysis was performed on rabbit soleus muscle in order to determine the amount of slow myosin heavy chain type I (MHC I) present and its ratio to other myosin isotypes.
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