Anti-Human/Mouse/Rat AGA Polyclonal Antibody

Categories: [ Antibodies][ Polyclonal Antibodies]

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.

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Properties

Data Sheet	Click for Datasheet
Catalog Number	PA13004
Size	100μl
Host Type	Rabbit
Immunogen	Recombinant protein of human AGA
Specificity
Isotype	IgG
Reacitivity	Human,Mouse,Rat
Clone
Uniprot	P20933
Concentration	0.2 mg/mL
Dilution	WB 1:200-1:1000, IHC 1:15-1:50
Formulation
Application	WB,IHC,ELISA
Other Names	GA,AGU,ASRG
Storage	Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript	For research use only, not for use in diagnostic procedures.

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Anti-Human/Mouse/Rat AGA Polyclonal Antibody

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