MFGM Polyclonal Antibody, 20ul Metabolic enzymes This gene is mutated in

This gene is mutated in congenital disorder of glycosylation type Ik

An important paralog of this gene is WBSCR16

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

The central feature of PAX5 family is a novel

This promotes neural repair after stroke

MFGM Polyclonal Antibody, 20ul Metabolic enzymes This gene is mutated inThis 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