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Human von willebrand factor (factor viii r:ag) is a 270 kda multimeric plasma gylcoprotein Suitable for human, mouse, pig. The von willebrand factor has functional binding domains to platelet glycoprotein ib, glycoprotein iib/iiia, collagen and heparin.
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A pericyte marker in red. Results aid in the classification of acute myeloid leukemia fab type. Description von willebrand factor (vwf) plays a crucial role in blood clotting by assisting platelets in forming clots at the site of blood vessel injury
Acting as a bridge between platelets and the damaged blood vessel walls, vwf facilitates platelet adhesion and aggregation, which are essential steps in the clotting process.
Expression of the von willebrand factor gene is tissue specific and confined to endothelial cells and megakaryocytes
