| Code | EK1452 |
| Brand | Boster |
| Title | Human IDS/Iduronate 2 Sulfatase PicoKine"! ELISA Kit |
| Description | Human IDS/Iduronate 2 Sulfatase PicoKine”! ELISA Kit |
| Size | 1 x 96T |
| alternative_name | Iduronate 2-sulfatase |
| Scheda prodotto | www.bosterbio.com/datasheet.php?sku=EK1452 |
| general_information | Iduronate 2-sulfatase (IDS) is a sulfatase enzyme associated with Hunter syndrome. It encodes a member of the sulfatase family of proteins. Iduronate 2-sulfatase is involved in the lysosomal degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. |
| protein_id | P22304 |
| range_detection | 156pg/ml-10000pg/ml |
| sensitivity | <15pg/ml |
| storage | Store at 4Ú C for 6 months, at -20Ú C for 12 months. Avoid multiple freeze-thaw cycles(Shipped with wet ice.) |
| Detection method | ELISA |
| Sample Type | cell culture supernates, cell lysates, serum and plasma (heparin, EDTA). |
| Target species | Hu |
| Assay type | complete kit |
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