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Aspartylglucosylamine Deaspartylase (AGA) Antibody
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Catalogue No: abx004855
Price:
US$217.50
(Size: 20 µl)
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AGA Antibody is a Rabbit Polyclonal antibody against AGA. 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.
Research Articles on Aspartylglucosylamine Deaspartylase (AGA)
| Target | Aspartylglucosylamine Deaspartylase (AGA) |
| Clonality | Polyclonal |
| Reactivity | Human, Mouse |
| Tested Applications | ELISA, WB |
| Host | Rabbit |
| Recommended dilutions | ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user. |
| Conjugation | Unconjugated |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 161-346 of human AGA. |
| Isotype | IgG |
| Form | Liquid |
| Purification | Purified by affinity chromatography. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| UniProt Primary AC | P20933 (UniProt, ExPASy) |
| UniProt Secondary AC | B2R7H2, D3DP47, Q4W5Q2, Q6FHN6, Q9UCK6, Q9UCK7, Q9UCK8 |
| UniProt Entry Name | ASPG_HUMAN |
| Gene Symbol | AGA |
| GeneID | 175 |
| NCBI Accession | NP_000018.2 |
| KEGG | hsa:175 |
| String | 9606.ENSP00000264595 |
| Molecular Weight | Calculated MW: 37 kDa Observed MW: 37 kDa |
| Buffer | PBS, pH 7.3, containing 0.01% thimerosal, 50% glycerol. |
| Concentration | > 0.2 mg/ml |
| Availability | Shipped within 5-10 working days. |
| Note | THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION. |