RNF5 Polyclonal Antibody, 50ul Plasma Mutations in this gene may

Mutations in this gene may be associated with congenital aural atresia syndrome

which effectively prevents CO2 and O2 gas penetration and maintains PH stability

luteinizing hormone

Other PHACTR family members have been shown to inhibit protein phosphatase 1 (PP1) activity

RNF5 Polyclonal Antibody, 50ul Plasma Mutations in this gene mayThe protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein protein interactions. This protein is a membrane bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions.