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Invitrogen™ AGA Polyclonal Antibody
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Catalog No. PA550309
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100 μL
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PA550309 100 μL
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Catalog No. PA550309 Supplier Invitrogen™ Supplier No. PA550309
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Rabbit Polyclonal Antibody

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.
TRUSTED_SUSTAINABILITY

Specifications

Antigen AGA
Applications Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 0.8 mg/mL
Conjugate Unconjugated
Formulation PBS with 40% glycerol and 0.05% sodium azide; pH 7.4
Gene Aga
Gene Accession No. P20933, Q64191
Gene Alias Aga; AGU; Aspartylglucosaminidase; aspartylglucosylamine deaspartylase; ASRG; AW060726; GA; Glycosylasparaginase; Glycosylasparaginase alpha chain; Glycosylasparaginase beta chain; N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase; N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase
Gene Symbols Aga
Host Species Rabbit
Immunogen Fusion protein corresponding to a region derived from internal residues of human Aspartylglucosaminidase.
Purification Method Antigen affinity chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 11593, 175
Target Species Human, Mouse
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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WARNING: Cancer - www.P65Warnings.ca.gov
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