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Description
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. [provided by RefSeq
Specifications
Specifications
| Antigen | AGA |
| Applications | Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Mouse polyclonal antibody raised against a full-length human AGA protein. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | AGA |
| Gene Accession No. | NM_000027.2 |
| Gene Alias | AGU/ASRG/GA |
| Gene Symbols | AGA |
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