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,Rat
Applications：IHC
Concentration：1.1 mg/mL
Immunogen：KLH conjugated Synthetic peptide corresponding to Mouse VWF
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.02％ sodium azide,100 ug/ml BSA and 50％ glycerol.
