| No | Size | Price | Availability | |
| ARP175-01 | 50ul | 1500.00 | In Stock |  |
| ARP175-01 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 175 |
| Isotype: | IgG | Swiss Prot: | P20933 |
| purity: | Affinity purification |
| Background: |
| 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. |
| Reactivity | Human, Mouse |
| Tested applications | WB IHC IF |
| Clonality | Polyclonal Antibody |
| Calculated MW | 37kDa |
| Recommended Dilutions |
WB 1:500 - 1:2000
IHC 1:50 - 1:200
IF 1:50- 1:100
|
| Immunogen | A recombinant protein of human AGA |
| Storage | Store at -20oC (regular) or -80oC (long term). Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| Synonym | GA, AGU, ASRG |
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