Adamts2 Antikörper

Produktnummer ABIN7255235

Produktdetails anti-Adamts2 Antikörper

Target: Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Adamts2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of mouse ADAMTS2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu Adamts2

Target: Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))

Andere Bezeichnung: ADAMTS2 (Adamts2 Produkte)

Synonyme: ADAM-TS2 antikoerper, ADAMTS-2 antikoerper, ADAMTS-3 antikoerper, PCINP antikoerper, hPCPNI antikoerper, mKIAA4060 antikoerper, pNPI antikoerper, NPI antikoerper, PC I-NP antikoerper, PCI-NP antikoerper, PCPNI antikoerper, PNPI antikoerper, RGD1565950 antikoerper, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 2 antikoerper, ADAM metallopeptidase with thrombospondin type 1 motif 2 antikoerper, ADAM metallopeptidase with thrombospondin type 1 motif, 2 antikoerper, Adamts2 antikoerper, ADAMTS2 antikoerper

Hintergrund: This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.

Molekulargewicht:

Observed_MW: 120 kDa

Calculated_MW: 61 kDa/134 kDa

Gen-ID: 216725

UniProt: Q8C9W3