IMDH1 Rabbit Polyclonal Antibody, 50ul Biomatrix The protein encoded by this

The protein encoded by this gene is a member of the cyclin-dependent serine/threonine protein kinase family

Mutations in CYP7B1 have been associated with hereditary spastic paraplegia (SPG5 or HSP)

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

this cleavage can release bioactive molecules from the extracellular matrix

also known as DCLK3 or DCDC3C

IMDH1 Rabbit Polyclonal Antibody, 50ul Biomatrix The protein encoded by thisThe 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.