MYL2 Monoclonal Antibody, 50ul Vortex Mixer AMPD2 and AMPD3

AMPD2 and AMPD3

This protein is phosphorylated

Caffey Disease and idiopathic osteoporosis

and is thought to function as an ATP-dependent RNA helicase that regulates the release of spliced mRNAs from spliceosomes prior to their export from the nucleus

that are preferentially activated by adenosine and uridine nucleotides

MYL2 Monoclonal Antibody, 50ul Vortex Mixer AMPD2 and AMPD3Thus 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.