Product Type: Antibody
Descritpion: 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.
Recommended Dilutions: WB 1:200-1:1000, IHC 1:15-1:50
Size: 200 uL
Gene Accession: BC012392
Immunogen: Recombinant protein of human AGA
Formulation: PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Purification: Affinity purification
Calculated MW: 37kDa
Tissue Specificity/Positive Control:
Cellular Localization: Endoplasmic reticulum,endoplasmic reticulum,Extracellular region or secreted,extracellular exosome,extracellular region,extracellular space,Lysosome,azurophil granule lumen,lysosome
Storage: Store at -20C. Avoid freeze / thaw cycles.