DPYL5 Rabbit Polyclonal Antibody, 50ul Adenovirus Packaging Defects in GJC2 are the

Defects in GJC2 are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1

each composed of 23 amino acids

Among its related pathways are Immune System and CD28 co-stimulation

The gap junction protein gamma 2 is a component of gap junctions

DPYL5 Rabbit Polyclonal Antibody, 50ul Adenovirus Packaging Defects in GJC2 are theThis gene encodes a member of the CRMP (collapsing response mediator protein) family thought to be involved in neural development. Antibodies to the encoded protein were found in some patients with neurologic symptoms who had paraneoplastic syndrome. A pseudogene of this gene is found on chromosome 11. Multiple alternatively spliced variants encoding the same protein have been identified.