ADAMTS2 Rekombinanter Antikörper
ADAMTS2 Rekombinant Antikörper für WB, IF/ICC, Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human
Anwendung
WB, IF/ICC, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
241860B8
Kat-Nr. : 84476-6-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
84476-6-PBS bindet in WB, IF/ICC, Indirect ELISA ADAMTS2 und zeigt Reaktivität mit human
| Getestete Reaktivität | human |
| Wirt / Isotyp | Kaninchen / IgG |
| Klonalität | Rekombinant |
| Typ | Antikörper |
| Immunogen | ADAMTS2 fusion protein Ag34957 |
| Vollständiger Name | ADAM metallopeptidase with thrombospondin type 1 motif, 2 |
| Berechnetes Molekulargewicht | 135 kDa |
| Beobachtetes Molekulargewicht | 110~130 kDa |
| GenBank-Zugangsnummer | NM_014244 |
| Gene symbol | ADAMTS2 |
| Gene ID (NCBI) | 9509 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein A purfication |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
A disintegrin and metalloproteinase with thrombospondin motifs 2 (ADAMTS-2) is a metalloproteinase that plays a key role in the processing of fibrillar procollagen precursors into mature collagen molecules by excising the amino-propeptide. ADAMTS-2 can, like the procollagen C-proteinases, be regulated by transforming growth factor-β1 (TGF-β1), with implications for mechanisms whereby this growth factor effects net increases in formation of extracellular matrix. Mutations in the ADAMTS-2 gene cause dermatosparaxis in human (dermatosparactic type of Ehlers-Danlos syndrome, also known as Ehlers-Danlos syndrome type VIIC). Human ADAMTS-2 has eight potential sites for Asn-linked glycosylation and other mammals (PMID: 16046392, 12646579).





