Factor XII (F.XII, Hageman factor) is a 76kD, single chain glycoprotein produced in the liver. In plasma, F.XII circulates as a protease zymogen at a concentration of~30ug/ml (400nM). Upon vascular injury F.XII binds to negatively charged extravascular surfaces such as cartilage and skin, which facilitate activation of the zymogen to the active serine protease. Cleavage of F.XII by kallikrein after residue Arg353 produces the enzyme alapha F.XIIa, consisting of a 28kD light chain containing the protease domain, and a 52kD heavy chain containing the anionic surface-binding domain. Substrates for surface bound F.XIIa include the zymogens prekallikrein (PK) and factor XI (F.XI) as well as the procofactor high-molecular weight kininogen (HK). The activation of these substrates results in positive feedback activation of F.XII. Further cleavage of alpha F.XIIa by kallikrein produces the 28kD fragment beta F.XIIa (hageman factor fragment). beta F.XIIa has reduced procoagulant activity as it lacks the anionic surface-binding domain, but is capable of fluid-phase activation of PK, factor VII and complement C1. The activity of F.XIIa in plasma is regulated predominantly by C1-Inhibitor, with relatively minor contributions by alpha 2antiplasmin, alpha 2macroglobulin and antithrombin, even in the presence of therapeutic levels of heparin.
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