Troponin T-C Polyclonal Antibody, 20ul Recombinant Protein Expression Mutations in this gene have

Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency)

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mis-segregation of sister chromatids

and they are referred to as cyclins A through I

Troponin T-C Polyclonal Antibody, 20ul Recombinant Protein Expression Mutations in this gene haveTroponin T cardiac muscle encoded by TNNT2 is the tropomyosin binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy. Transcripts for this gene undergo alternative splicing that