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

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

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

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

It can bind to anti-apoptotic Bcl-2 family members to induce mitochondrial dysfunction and caspase activation

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

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