PLOD2 Polyclonal Antibody, 100ul Supplements Its function has not been

Its function has not been determined

an autosomal recessive disorder characterized by conjugated hyperbilirubinemia

The protein is expressed in the photoreceptor layer of the retina| and the gene is mutated in autosomal recessive retinitis pigmentosa

This protein may have proton-sensing activity and may be a receptor for oxidized free fatty acids

PLOD2 Polyclonal Antibody, 100ul Supplements Its function has not beenThe protein encoded by this gene is a membrane bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers Danlos syndrome