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MYBPC2 encodes a member of the myosin-binding protein C family. Zusätzlich bieten wir Ihnen Myosin Binding Protein C, Fast Type Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal MYBPC2 Primary Antibody für EIA, IHC (p) - ABIN5555025
Emmanuele, Kubota, Garcia-Diaz, Garone, Akman, Sánchez-Gutiérrez, Escudero, Kariya, Homma, Tanji, Quinzii, Hirano: Fhl1 W122S causes loss of protein function and late-onset mild myopathy. in Human molecular genetics 2015
the mean methylation level of CpGs was significantly higher in MYBPC3 than MYBPC2.
The patients with a frameshift deletion mutation of MyBPC may develop LV systolic dysfunction and suffer from cardiovascular events through mid-life and beyond.
Identification of interactions between domains of Myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations.
the CD-loop is a natively unfolded sequence with a likely coupling between folding and ligand binding.
Role and quaternary structure of MyBPC in skeletal muscle.
The distribution of MyBP-C in the A-bands of cardiac and skeletal muscles and compare this to the A-band structure in cardiac muscle of MyBP-C-deficient mice, was investigated.
lack of MyBPC-2 results in a severe skeletal myopathy, elevated apoptosis and shorter sarcomeres.
This gene encodes a member of the myosin-binding protein C family. This family includes the fast-, slow- and cardiac-type isoforms, each of which is a myosin-associated protein found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. The protein encoded by this locus is referred to as the fast-type isoform. Mutations in the related but distinct genes encoding the slow-type and cardiac-type isoforms have been associated with distal arthrogryposis, type 1 and hypertrophic cardiomyopathy, respectively.
C-protein, skeletal muscle fast isoform
, fast MyBP-C
, fast-type C-protein
, myosin-binding protein C, fast-type
, fast-type muscle myosin-binding-protein C