DRP2 Rabbit Polyclonal Antibody, 20ul Pipette Holder Mutations in SLC39A4 result in

Mutations in SLC39A4 result in acrodermatitis enteropathica

mediate the trafficking and membrane organization of a number of transmembrane proteins

Mutations in CUBN may play a role in autosomal recessive megaloblastic anemia

The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family

E2F transcription factor 6 encoded by E2F6 lacks the transactivation and tumor suppressor protein association domains found in other family members

DRP2 Rabbit Polyclonal Antibody, 20ul Pipette Holder Mutations in SLC39A4 result inMembers of the dystrophin family of proteins perform a critical role in the maintenance of membrane associated complexes at points of intercellular contact in vertebrate cells. The protein encoded by this gene is predicted to resemble certain short C terminal isoforms of dystrophin and dystrophin related protein 1 (DRP1 or utrophin). DRP2 is expressed principally in the brain and spinal cord. Two transcript variants encoding different isoforms have