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Human von willebrand factor (factor viii r:ag) is a 270 kda multimeric plasma gylcoprotein Immunogen corresponding to native full length protein corresponding to human vwf. The von willebrand factor has functional binding domains to platelet glycoprotein ib, glycoprotein iib/iiia, collagen and heparin
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The factor is synthesized by endothelial cells and is also present in platelets and megakaryocytes. Rabbit polyclonal von willebrand factor antibody Vwf (von willebrand factor) is a multimeric plasma glycoprotein that promotes adhesion of platelets to sites of vascular injury (1)
It is synthesized as a large precursor protein and undergoes extensive.
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. A pericyte marker in red. Expression of the von willebrand factor gene is tissue specific and confined to endothelial cells and megakaryocytes
Results aid in the classification of acute myeloid leukemia fab type.
