AGA
aspartylglucosaminidase
AGU, ASRG, GA
Human AGA (175), Mouse Aga (11593), Rat Aga (290923), Zebrafish aga (566517), cow AGA (511345), domestic cat AGA (101086138), dog AGA (475638), chicken AGA (422558), naked mole-rat Aga (101721618), domestic guinea pig Aga (100724192)
- Human(175) Summary: 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. [provided by RefSeq, Jan 2010]
- Mouse(11593) aspartylglucosaminidase
- Rat(290923) aspartylglucosaminidase
- Zebrafish(566517) aspartylglucosaminidase
- cow(511345) aspartylglucosaminidase
- domestic cat(101086138) aspartylglucosaminidase
- dog(475638) aspartylglucosaminidase
- chicken(422558) aspartylglucosaminidase
- naked mole-rat(101721618) aspartylglucosaminidase
- domestic guinea pig(100724192) aspartylglucosaminidase
- sheep(101106396) aspartylglucosaminidase
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Antibodies
Anti-AGA antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
human
immunohistochemistry
Anti-AGA antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
human
immunohistochemistry