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

is a 165 amino acid protein encoded in the major histocompatibility complex (MHC) that consists of two domains which share significant homology with ubiquitin

eceptor that plays a critical role in lung surfactant homeostasis

The intermediate and light chains

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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.