AGA polyclonal, anti-human, mouse, rat

Background:
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.

Synonyms: GA, AGU, ASRG

Cellular Location: Cytoplasm

Immunogen:
Recombinant protein of human AGA

Gene Symbol: AGA

Gene ID: 175

Swiss prot: P20933

Calculated MW: 37kDa

Recommended dilution:
WB 1:200-1000, IHC 1:15-50,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.