Background：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.
仕様
Synonyms：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
Host：Rabbit
Reactivity：Human
Applications：IHC,ELISA
Concentration：0.4mg/mL
Immunogen：Recombinant protein of human VWF
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.05％ sodium azide, 50％ glycerol, PH7.3
