AMPD1 Polyclonal Antibody, 100ul Bio-Reaction Tube This gene encodes a member

This gene encodes a member of the WD repeat protein family

Mutations in this gene have been linked to hyperparathyroidism-jaw tumor syndrome

and functions in maintaining microtubule organization and cell morphology

Alternative splicing seems to be a common mechanism in this gene family

AMPD1 Polyclonal Antibody, 100ul Bio-Reaction Tube This gene encodes a memberAdenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver and erythocyte specific isoforms, respectively. Deficiency of the muscle specific enzyme is apparently a common cause of exercise induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively