The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22.

Codice: E-AB-70006_200μL | Marca: Elabscience | Confezionamento: 200μL

Specie: Human;RatIsotipo: IgGConiugazione: Unconjugated

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Codice: E-AB-70006_200μL
Marca: Elabscience
Specie target: Human;Rat
Host: Rabbit
Concentrazione: 1.1 mg/mL
Link: Apri link
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG
Clonalità: Polyclonal
Coniugazione: Unconjugated
Applicazione: IHC
Diluizione: IHC 1:200-1:800
Simbolo target: VWF
Ig target: Coagulation factor VIII;Coagulation factor VIII VWF;F8VWF;Factor VIII related antigen;von Willebrand antigen 2;von Willebrand antigen II;Von Willebrand disease;VWD;vWF;VWF
Area di ricerca: Cancer;Cardiovascular;Stem Cells

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