FAM5C Rabbit Polyclonal Antibody, 50ul Multiplex Immunoassays Defects in this gene are

Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease

MIM 603034)

and is safe and convenient to use The smallest bag of each product is marked with the batch number

This enzyme is a microsomal vitamin D hydroxylase that converts vitamin D into the active ligand for the vitamin D receptor

FBXO5 and probably NFKB2

FAM5C Rabbit Polyclonal Antibody, 50ul Multiplex Immunoassays Defects in this gene areThis gene is overexpressed in pituitary tumors but is underexpressed in tongue squamous cell carcinomas ulcerative colitis and peri implantitis. Polymorphisms that increase expression of this gene have been shown to increase vascular inflammation and an association of this gene with myocardial infarction has been demonstrated. Finally hypermethylation of this gene may find usefulness as a biomarker for gastric cancer. Two transcript variants encoding