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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Immunogen sequence: SSPLPLVVNT WPFKNATEAA WRALASGGSA LDAVESGCAM CEREQCDGSV
Highest antigen sequence identity to the following orthologs: Mouse - 86%, Rat - 84%.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: AGA; aspartylglucosylamine deaspartylase; glycosylasparaginase; mutated glycoasparaginase gene, deletion at bp 29; N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase; unnamed protein product
基因别名: AGU; ASRG; GA
UniProt ID: (Human) P20933
Entrez Gene ID: (Human) 175