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

Mutations in SLC39A4 result in acrodermatitis enteropathica

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

alpha-latrotoxin

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

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

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