Human von Willebrand factor (factor VIII R:Ag) is a 270kD multimeric plasma gylcoprotein. It mediates platelet adhesion to injured vessel walls and serves as a carrier and stabilizer for coagulation factor VIII. The von Willebrand factor has functional binding domains to platelet glycoprotein Ib, glycoprotein IIb/IIIa, collagen and heparin. The factor is synthesized by endothelial cells and is also present in platelets and megakaryocytes.
Applications:
Suitable for use in Immunofluorescence and Immunohistochemistry. Other applications not tested.
Recommended Dilution:
Immunohistochemistry (Paraffin): 1:200-1:400 using indirect Immunoflourescence. Enzymatically pre-digested with 0.1% pronase, formalin fixed. Specifically stains endothelial cells.
Immunohistochemistry (Paraffin): 1:1000 using indirect immunoperoxidase. Enzymatically pre-digested with 0.1% pronase, formalin fixed and developed with Biotin/Avidin. Specifically stains blood vessels.
Optimal dilutions to be determined by the researcher.
Positive Control:
Formalin-fixed, paraffin sections of human tongue
Storage and Stability:
May be stored at 4 degrees C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degrees C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.