ACY2 Rabbit Polyclonal Antibody, 100ul Enzyme Activity Assays Deletions in this gene may

Deletions in this gene may contribute to the etiology of velo-cardio-facial syndrome and DiGeorge syndrome

Individually wrapped

The encoded protein contains sequence and structural similarity to members of the neprilysin (M13) family of zinc endopeptidases

eceptor that plays a critical role in lung surfactant homeostasis

RPS2 encodes a ribosomal protein that is a component of the 40S subunit

ACY2 Rabbit Polyclonal Antibody, 100ul Enzyme Activity Assays Deletions in this gene mayThis gene encodes an enzyme that catalyzes the conversion of N acetyl_L aspartic acid (NAA) to aspartate and acetate. NAA is abundant in the brain where hydrolysis by aspartoacylase is thought to help maintain white matter. This protein is an NAA scavenger in other tissues. Mutations in this gene cause Canavan disease. Alternatively spliced transcript variants have been found for this gene.