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PLOD2 Polyclonal Antibody, 100ul Supplements an autosomal recessive disorder characterized

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PLOD2 Polyclonal Antibody, 100ul Supplements an autosomal recessive disorder characterizedThe 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

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Description

an autosomal recessive disorder characterized by conjugated hyperbilirubinemia

This cytokine is expressed in carcinoma cell lines

It is located in the cytoplasm as a ribosomal component

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

PLOD2 Polyclonal Antibody, 100ul Supplements an autosomal recessive disorder characterizedThe 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

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