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GNS Polyclonal Antibody, 100ul Metabolic enzymes is a lysosomal cysteine proteinase

SKU: 7301683346

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GNS Polyclonal Antibody, 100ul Metabolic enzymes is a lysosomal cysteine proteinaseThe product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

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Description

is a lysosomal cysteine proteinase that may play an important role in corneal physiology

and downregulation of it may serve as a good biomarker for predicting patient outcomes

Dephosphorylates NDEL1 at CDC2/Cdk1 phosphorylation sites and negatively regulates CDC2/Cdk1 activity in interphase

This gene encodes a member of the high sulfur-type keratin-associated protein (KAP) family

The encoded preproprotein is proteolytically processed to generate two proteins including the extracellular matrix component fibrillin-1 and the protein hormone asprosin

GNS Polyclonal Antibody, 100ul Metabolic enzymes is a lysosomal cysteine proteinaseThe product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

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