MYL2 Polyclonal Antibody, 50ul Vector Construction which shows stable performance

which shows stable performance

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

Mutations in this gene result in type 2 oculocutaneous albinism

an autosomal recessive disease associated with a susceptibility to pyogenic infections

Comes with an individually packaged centrifuge tube cap for easy storage

MYL2 Polyclonal Antibody, 50ul Vector Construction which shows stable performanceThus 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.