Products

Alglucerase (TP-016CL)

Human Beta-glucocerebrosidase or Beta-D-glucosyl-N-acylsphingosine glucohydrolase E.C. 3.2.1.45. 497 residue protein with N-linked carbohydrates, MW=59.3 kD. Alglucerase is prepared by modification of the oligosaccharide chains of human Beta-glucocerebrosidase. The modification alters the sugar residues at the non-reducing ends of the oligosaccharide chains of the glycoprotein so that they are predominantly terminated with mannose residues      

  • Datasheet

Specifications
Classify
Protein therapeutics replacing a protein that is deficient or abnormal: Metabolic enzyme deficiencies
Therapeutic
β-Gluco-cerebrosidase
Trade Name
Ceredase (Purified From Pooled Human Placenta)
Function
Hydrolyzes glucocerebroside to glucose and ceramide
Examples of Clinical Use
Gaucher's disease
References
Synonyms
Not Available
UniProt
P04062
Genbank
M16328

For lab research use only, not for diagnostic, therapeutic or any in vivo human use.

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