CCD50 Rabbit Polyclonal Antibody, 100ul Protein Research This cyclin forms a complex

This cyclin forms a complex with CDK4 or CDK6 and functions as a regulatory subunit of the complex

Mutations in this gene and H6PD (hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)) are the cause of cortisone reductase deficiency

with high affinity

Expressed ubiquitously in tissues including liver

CCD50 Rabbit Polyclonal Antibody, 100ul Protein Research This cyclin forms a complexThis gene encodes a soluble, cytoplasmic, tyrosine phosphorylated protein with multiple ubiquitin interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule based structures. This protein may also function as a negative regulator of NF kB signaling and as an