Fucokinase Monoclonal Antibody, 100ul Purification a common congenital disorder characterized

a common congenital disorder characterized by neural-crest-related developmental defects

and resides in the endoplasmic reticulum (ER)

Mutations in this gene have been associated with noninsulin-dependent diabetes mellitus (NIDDM)

induction:By IL6

and a minor mediator of the JNK pathway

Fucokinase Monoclonal Antibody, 100ul Purification a common congenital disorder characterizedThe protein encoded by this gene belongs to the GHMP (galacto , homoserine, mevalonate and phosphomevalonate) kinase family and catalyzes the phosphorylation of L fucose to form beta L fucose 1 phosphate. This enzyme catalyzes the first step in the utilization of free L fucose in glycoprotein and glycolipid synthesis. L fucose may be important in mediating a number of cell cell interactions such as blood group antigen recognition, inflammation, and