Native Human Troponin I (Cardiac)
Human cardiac troponin I is the inhibitory subunit of troponin involved in confering calcium sensitivity to muscle actomyosin ATPase activity. Mutation of the TNN13 gene can lead to familial hypotrophic cardiomyopathy 7 (CMH7), a hereditary heart condition characterized by asymetric ventricular hypertrophy (Kimura et al. 1997). Other cardiomyopathies also occur as a result of mutations in the TNN13 gene (UniProt : P19429).
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Native Human Troponin I (Cardiac)
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Native Human Troponin I (Cardiac)
9202-0707
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