FAM5C Rabbit Polyclonal Antibody, 50ul Multiplex Immunoassays FBXO5 and probably NFKB2

FBXO5 and probably NFKB2

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

lacks a 5' terminal insert

Multiple alternatively spliced transcript variants encoding different isoforms have been identified in CD4

This difference in size is largely due to an increase in the number of subdomains

FAM5C Rabbit Polyclonal Antibody, 50ul Multiplex Immunoassays FBXO5 and probably NFKB2This 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