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AGA Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Marque: Proteintech 17299-1-AP-20UL
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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. Alternatively spliced transcript variants have been identified.Spécification
| AGA | |
| Polyclonal | |
| Unconjugated | |
| AGA | |
| AGA, AGU, aspartylglucosaminidase, ASRG, GA, Glycosylasparaginase | |
| Rabbit | |
| Antigen Affinity Chromatography | |
| RUO | |
| 11593, 175, 290923 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 0.23 mg/mL | |
| PBS with 50% glycerol and 0.1% sodium azide; pH 7.3 | |
| P20933, P30919, Q64191 | |
| Aga | |
| AGA Fusion Protein Ag10681 | |
| 20 μL | |
| Primary | |
| Rat, Mouse, Human | |
| Antibody | |
| IgG |
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