This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22.

Codice: AN300869L_50μL | Marca: Elabscience | Confezionamento: 50μL

Specie: Human;Mouse;RatIsotipo: IgG,κClone: 9B6Coniugazione: Unconjugated
Dettagli prodotto
  • Codice: AN300869L_50μL
  • Marca: Elabscience
  • Specie target: Human;Mouse;Rat
  • Host: Rabbit
  • Concentrazione: 0.2 mg/mL
  • Link: Apri link
  • Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
  • Isotipo: IgG,κ
  • Clonalità: Monoclonal;Recombinant
  • Clone: 9B6
  • Coniugazione: Unconjugated
  • Applicazione: WB;IHC
  • Diluizione: IHC 1:1000-1:4000;WB 1:2000-1:10000
  • Simbolo target: VWF
  • Ig target: von Willebrand antigen;VWF;F8VWF;VWD;Coagulation factor VIII;Coagulation factor VIII VWF;Factor VIII related antigen;von Willebrand antigen 2;von Willebrand antigen II;Von Willebrand disease;Von Willebrand Factor
  • Area di ricerca: Cardiovascular;Cancer;Stem Cells