IMDH1 Rabbit Polyclonal Antibody, 50ul Biomatrix also known as DCLK3 or

also known as DCLK3 or DCDC3C

This autosomal dominant disorder is characterized by abnormal water reabsorption by kidney tubules due

also referred to as Parkinson disease 9

and expressed in testis and in a significant fraction of tumors of various histological types

Regulates inositol phosphate metabolism by phosphorylation of second messenger inositol 1

IMDH1 Rabbit Polyclonal Antibody, 50ul Biomatrix also known as DCLK3 orThe protein encoded by this gene acts as a homotetramer to regulate cell growth. The encoded protein is an enzyme that catalyzes the synthesis of xanthine monophosphate (XMP) from inosine 5' monophosphate (IMP). This is the rate limiting step in the de novo synthesis of guanine nucleotides. Defects in this gene are a cause of retinitis pigmentosa type 10 (RP10). Several transcript variants encoding different isoforms have been found for this gene.