DRP2 Rabbit Polyclonal Antibody, 20ul Pipette Holder Mutations in CUBN may play

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

with alpha actins being a major constituent of the contractile apparatus

Due to the sequence and biochemical similarities with the RB1 protein

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

DRP2 Rabbit Polyclonal Antibody, 20ul Pipette Holder Mutations in CUBN may playMembers 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