PRDX5 Polyclonal Antibody, 20ul Electronic Pipette chromosomal aberrations involving this gene

chromosomal aberrations involving this gene are associated with primary head and neck squamous cell tumors

Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II| also known as Hunter syndrome

eta-adrenergic receptors mediate the catecholamine-induced activation of adenylate cyclase through the action of G proteins

It interacts with the centrosomal proteins aurora-A and ajuba and is required for accumulation of gamma-tubulin and spindle formation at the onset of mitosis

whose members interact with outer kinetochore proteins and help to maintain centromere identity at each cell division cycle

PRDX5 Polyclonal Antibody, 20ul Electronic Pipette chromosomal aberrations involving this geneThis gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein may play an antioxidant protective role in different tissues under normal conditions and during inflammatory processes. This protein interacts with peroxisome receptor 1. The crystal structure of this protein in its reduced form has been resolved to 1. 5 angstrom resolution. This gene uses