MYH7B Rabbit Polyclonal Antibody, 50ul Adeno-associated Virus Packaging The peroxisome biogenesis disorders (PBDs)

The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive

It is involved in energy metabolism

Mutations in PHYKPL (5-phosphohydroxy-L-lysine phospho-lyase) may cause phosphohydroxylysinuria

Expression of PMEPA1 is induced by androgens and transforming growth factor beta

and cellular activation and has been linked to Gray platelet syndrome

MYH7B Rabbit Polyclonal Antibody, 50ul Adeno-associated Virus Packaging The peroxisome biogenesis disorders (PBDs)The myosin II molecule is a multi subunit complex consisting of two heavy chains and four light chains. This gene encodes a heavy chain of myosin II which is a member of the motor domain superfamily. The heavy chain includes a globular motor domain which catalyzes ATP hydrolysis and interacts with actin and a tail domain in which heptad repeat sequences promote dimerization by interacting to form a rod like alpha helical coiled coil. This heavy chain