MCP Polyclonal Antibody, 100ul Endonucleases & Exonucleases Deletions of portions of the

Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia

subcellular location:Associated with perinuclear vesicles

Interacts with KFL1 (By similarity)

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

MCP Polyclonal Antibody, 100ul Endonucleases & Exonucleases Deletions of portions of theThe 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,