Anti-Human VWF Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12853
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human VWF
Specificity Plasma.
Isotype IgG
Reacitivity Human
Clone
Uniprot P04275
Concentration 0.4 mg/mL
Dilution IHC 1:25-1:100
Formulation
Application IHC,ELISA
Other Names 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
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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