• Product NameRecombinant Human AGA
• Brief DescriptionRecombinant Protein
• Immunogen DescriptionFusion protein corresponding to a region derived from 206-346 amino acids of human aspartylglucosaminidase
• Target NameAspartylglucosaminidase
• Alternative Names    GA; AGU; ASRG
• Accession No. Swissprot:P20933
  Gene Accession:BC012392
• UniprotP20933
• Gene ID175;
• Storage -20~-80˚C, pH 7.6 PBS

Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. Alternatively spliced transcript variants have been identified.?

Note: For in vitro research use only, not for diagnostic or therapeutic use. This product is not a medical device.

• Flow Cytometry (FCM) General Protocol
• Immunofluorescence(IC)
• Immunohistochemistry(Polymer)
• Western Blotting