DRP2 Rabbit Polyclonal Antibody, 20ul Pipette Holder GlcNAcalpha1-->4Galbeta-->R and is largely associated

GlcNAcalpha1-->4Galbeta-->R and is largely associated with the Golgi apparatus membrane

including exocytosis

Mutations in SLC39A4 result in acrodermatitis enteropathica

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

alpha-latrotoxin

DRP2 Rabbit Polyclonal Antibody, 20ul Pipette Holder GlcNAcalpha1-->4Galbeta-->R and is largely associatedMembers 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