MYL3 Polyclonal Antibody, 50ul Immune Cell Analysis Hereditary hemorrhagic telangiectasia

Hereditary hemorrhagic telangiectasia

It has been identified that genetic variation in this gene plays a role in the determination of bone mineral density (BMD)

The protein encoded by this gene belongs to the glutamine synthetase family

The V1 domain consists of three A| three B| and two G subunits| as well as a C| D| E| F| and H subunit

The encoded protein has an N-terminal forkhead-associated domain

MYL3 Polyclonal Antibody, 50ul Immune Cell Analysis Hereditary hemorrhagic telangiectasiaMYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid left ventricular chamber type hypertrophic cardiomyopathy.