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AGA Rabbit anti-Human, Mouse, Polyclonal, Invitrogen™

Rabbit Polyclonal Antibody

Manufacturer:  Invitrogen PA550309

Catalog No. PA550309


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Description

Description

The antibody detects endogenous levels of total AGA protein.

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.
Specifications

Specifications

AGA
Polyclonal
Unconjugated
AGA
Liquid
AGA
Fusion protein corresponding to a region derived from internal residues of human Aspartylglucosaminidase
Antigen affinity chromatography
RUO
Antibody
Polyclonal
Human, Mouse
Immunohistochemistry (Paraffin), Western Blot
0.8 mg/mL
PBS with 50% glycerol and 0.05% sodium azide; pH 7.3
P20933, Q64191
GA, AGU, ASRG
Rabbit
IgG
100 μL
-20°C
Primary
11593, 175
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