Invitrogen™ AGA Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA550309

Catalog No. PA550309

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

• Antigen: AGA
• Classification: Polyclonal
• Conjugate: Unconjugated
• Gene: Aga
• 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
• Host Species: Rabbit
• Purification Method: Antigen affinity chromatography
• Regulatory Status: RUO
• Gene ID (Entrez): 11593, 175
• Content And Storage: -20°C
• Form: Liquid

• Applications: Immunohistochemistry (Paraffin), Western Blot
• Concentration: 0.8 mg/mL
• Formulation: PBS with 40% glycerol and 0.05% sodium azide; pH 7.4
• Gene Accession No.: P20933, Q64191
• Gene Symbols: Aga
• Immunogen: Fusion protein corresponding to a region derived from internal residues of human Aspartylglucosaminidase.
• Quantity: 100 μL
• Primary or Secondary: Primary
• Target Species: Human, Mouse
• Product Type: Antibody
• Isotype: IgG

Safety and Handling

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