GNS Polyclonal Antibody, 100ul Metabolic enzymes and downregulation of it may

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

Other family members are known to function in post-transcriptional regulation

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

as well as with NM23-1

GNS Polyclonal Antibody, 100ul Metabolic enzymes and downregulation of it mayThe 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.