Murine Anti-Factor VIII
Factor VIII (FVIII) is a heterodimer consisting of a heavy chain (ranging in mass from 90 to 200 kDa) bound via metal ions to a light chain (80 kDa). In plasma, FVIII circulates in an inactive form bound to von Willebrand factor. Following activation by factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8006 (also known as 2-77)1 recognizes the C2 domain of FVIII and strongly inhibits FVIII activation. It is suitable for flow cytometry2, ELISA, bio-layer interferometry pairing, and surface plasmon resonance experiments.3
- Species Reactivity:Human
- Specificity:C2 domain
- Immunogen:B-domain deleted recombinant Human Factor VIII
- ELISA:Binds the C2 domain of recombinant human factor VIII in solid-phase ELISA.
- Immunoblotting:Not recommended
- Inhibition:Strongly inhibitory in aPTT clotting assay.1
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- G.S. Pandey, C. Yanover, L.M. Miller-Jenkins, S. Garfield, S.A. Cole, J.E. Curran, E.K. Moses, N. Rydz, V. Simhadri, C. Kimchi-Sarfaty, D. Lillicrap, K. Viel, T.M. Przytycka, G.F. Pierce, T.E. Howard, Z.E. Sauna. (2013). Nat Med. 19(10):1318–1324
- P.T. Nguyen, K.B. Lewis, R.A. Ettinger, J.T. Schuman, J.C. Lin, J.F. Healey, S.L. Meeks, P. Lollar, K.P. Pratt. (2014). Blood. 123(17):2732-2739.
$240.00 – $600.00