Provided is a mouse monoclonal antibody, m82D6A3, directed against the von Willebrand factor (VWF) A3-domain, which inhibits the VWF-interaction to fibrillar collagen. The antibody 82D6A3 has antithrombotic effects in vivo.
Figure 1 Inhibition of VWF-binding to human collagen type III.
Before addition to collagen coated wells, a constant concentration of purified human VWF (250 ng/ml) was pre-incubated with different concentrations of purified h82D6A3 or m82D6A3. Bound VWF was detected with anti-VWF-HRP antibodies. The absorbance of VWF-binding in the absence of 82D6A3 was arbitrarily set as 0% inhibition.
Staelens, S., Desmet, J., Ngo, T. H., Vauterin, S., Pareyn, I., Barbeaux, P., ... & Vanhoorelbeke, K. (2006). Humanization by variable domain resurfacing and grafting on a human IgG4, using a new approach for determination of non-human like surface accessible framework residues based on homology modelling of variable domains. Molecular immunology, 43(8), 1243-1257.
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• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production
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ZG-507C | Mouse Anti-VWF Recombinant Antibody (clone RU8) | ELISA, immunopurification of vWF | Mouse IgG1, κ |
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