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

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

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

Ergonomic Design: Its lightweight streamlined design is ergonomically engineered to reduce fatigue and increase efficiency during extended use

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

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.