MCP Polyclonal Antibody, 100ul Endonucleases & Exonucleases and cataract)

and cataract)

Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB)

subcellular location:Associated with perinuclear vesicles

tissue specificity:Detected in hypopharyngeal head and neck squamous cell carcinoma

MCP Polyclonal Antibody, 100ul Endonucleases & Exonucleases and cataract)The protein encoded by this gene is a type I membrane protein and is a regulatory part of the complement system. The encoded protein has cofactor activity for inactivation of complement components C3b and C4b by serum factor I, which protects the host cell from damage by complement. In addition, the encoded protein can act as a receptor for the Edmonston strain of measles virus, human herpesvirus 6, and type IV pili of pathogenic Neisseria. Finally,