AMPD1 Polyclonal Antibody, 50ul Mini dry bath it is localized to the

it is localized to the mitochondria

Related pseudogenes have been found on chromosomes 3 and 14

Functions as a specific membrane receptor for beta-alanine

and a tyrosine phosphorylation site

This gene plays a role in DNA interstrand cross-link repair and encodes a protein with 5' flap endonuclease and 5'-3' exonuclease activity

AMPD1 Polyclonal Antibody, 50ul Mini dry bath it is localized to theAdenosine 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