MYBPC1 Polyclonal Antibody, 100ul Protein Research Defects in this gene are

Defects in this gene are a cause of dwarfism| while hypersecretion of the encoded protein is a cause of gigantism

Thr-312 is likely to be the main autophosphorylation site

Can interact with G/C-rich motifs from serotonin receptor promoter

TGFBR2 encodes a member of the Ser/Thr protein kinase family and the TGFB receptor subfamily

and E exhibiting the highest degree of conservation

MYBPC1 Polyclonal Antibody, 100ul Protein Research Defects in this gene areMYBPC1 encodes a member of the myosin binding protein C family. Myosin binding protein C family members are myosin associated proteins found in the cross bridge bearing zone (C region) of A bands in striated muscle. The encoded protein is the slow skeletal muscle isoform of myosin binding protein C and plays an important role in muscle contraction by recruiting muscle type creatine kinase to myosin filaments. Mutations in this gene are associated with