MFGM Polyclonal Antibody, 20ul Metabolic enzymes a disease associated with an

a disease associated with an heterogeneous group of cerebellar disorders

This gene is mutated in congenital disorder of glycosylation type Ik

miscellaneous:This protein has one functional calcium-binding site

Defects in this gene can also cause cone-rod dystrophy type 11| a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity| followed by the degeneration of rod photoreceptor cells| which progresses to night blindness and the loss of peripheral vision

Mutations in this gene result in Crigler-Najjar syndromes types I and II and in Gilbert syndrome

MFGM Polyclonal Antibody, 20ul Metabolic enzymes a disease associated with anThis gene encodes a preproprotein that is proteolytically processed to form multiple protein products. The major encoded protein product, lactadherin, is a membrane glycoprotein that promotes phagocytosis of apoptotic cells. This protein has also been implicated in wound healing, autoimmune disease, and cancer. Lactadherin can be further processed to form a smaller cleavage product, medin, which comprises the major protein component of aortic medial