Description: | The AGA (Aspartylglucosaminidase) protein functions as an enzyme that plays a crucial role in glycoprotein processing by cleaving the GlcNAc-Asn bond, which links oligosaccharides to the peptide chain of asparagine-linked glycoproteins. This cleavage action represents AGA's specificity in removing the N-linked glycan structures from glycoproteins, a process essential for the maturation and modification of these proteins. AGA's enzymatic activity at the GlcNAc-Asn bond contributes to the dynamic regulation of glycoprotein structure and function, influencing various physiological processes where N-linked glycosylation plays a pivotal role. AGA/Aspartylglucosaminidase Protein, Human (HEK293, His) is the recombinant human-derived AGA/Aspartylglucosaminidase protein, expressed by HEK293 , with C-10*His labeled tag. The total length of AGA/Aspartylglucosaminidase Protein, Human (HEK293, His) is 323 a.a., with molecular weight of ~47 & 29 & 23 & 20 kDa, respectively. |