PRDX5 Polyclonal Antibody, 20ul Electronic Pipette |disease:Defects in C1S are the

|disease:Defects in C1S are the cause of selective C1s deficiency

a single transmembrane domain

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

MAD2 is a key component of the spindle checkpoint that delays the onset of anaphase until all the kinetochores are attached to the spindle

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

PRDX5 Polyclonal Antibody, 20ul Electronic Pipette |disease:Defects in C1S are theThis 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