MYL2 Polyclonal Antibody, 50ul Vector Construction Mutations in this gene result

Mutations in this gene result in type 2 oculocutaneous albinism

Loss of function of the related gene in mouse results in a disruption of iron homeostasis between the mitochondria and cytosol

The membrane-associated protein encoded by this gene is included in the superfamily of ATP-binding cassette (ABC) transporters

proteins of the ribosome

MYL2 Polyclonal Antibody, 50ul Vector Construction Mutations in this gene resultThus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain. Ca+ triggers the phosphorylation of regulatory light chain that in turn triggers contraction. Mutations in this gene are associated with mid left ventricular chamber type hypertrophic cardiomyopathy.