Anti-VWF (Von Willebrand Factor)

Description:
Von Willebrand factor (vWF) is a blood glycoprotein involved in hemostasis. It is deficient or defective in von Willebrand disease and is involved in a large number of other diseases, including thrombotic thrombocytopenic purpura, Heyde's syndrome, and possibly hemolytic-uremic syndrome.
Von Willebrand factor is not an enzyme and, therefore, has no catalytic activity. Its primary function is binding to other proteins, in particular Factor VIII and it is important in platelet adhesion to wound sites.

Storage: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.