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

ADAMTS-2, pNPI, PCPNI, PCINP, ADAMTS 2



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 Molekulargewicht135 kDa
Beobachtetes Molekulargewicht110~130 kDa
GenBank-ZugangsnummerNM_014244
Gene symbol ADAMTS2
Gene ID (NCBI) 9509
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein A purfication
Lagerungspuffer PBS only
LagerungsbedingungenStore 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).