Invitrogen
Catalog # PA5-50309
Quantity:
TESTED APPLICATIONS | DILUTION |
---|---|
Immunohistochemistry (Paraffin) (IHC (P)) | 1:15-1:50 |
Western Blot (WB) | 1:200-1:1,000 |
Species reactivity | Human, Mouse |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | Fusion protein corresponding to a region derived from internal residues of human Aspartylglucosaminidase |
Conjugate | Unconjugated |
Form | Liquid |
Concentration | 0.8 mg/mL |
Purification | Antigen affinity chromatography |
Storage buffer | PBS, pH 7.4, with 40% glycerol |
Contains | 0.05% sodium azide |
Storage conditions | -20°C |
RRID | AB_2635762 |
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: AGA; Aspartylglucosaminidase; aspartylglucosylamine deaspartylase; Glycosylasparaginase; N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase; N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase
Gene Aliases: AGA; AGU; ASRG; AW060726; GA
UniProt ID: (Human) P20933, (Mouse) Q64191
Entrez Gene ID: (Human) 175, (Mouse) 11593
Molecular Function:
protease
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