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Coagulation Factor IX Human is a purified protein derived from human plasma that plays a critical role in the blood clotting cascade. It is essential for hemostasis and normal blood clotting as it acts as a zymogen (inactive enzyme precursor) that is activated by Coagulation Factor XIa to become an active serine protease. Once activated (Factor IXa), it forms a complex with calcium ions, membrane phospholipids, and Coagulation Factor VIII to activate Coagulation Factor X—an integral step in the formation of fibrin clots. Deficiency of this protein causes hemophilia B (Christmas disease). Therapeutic preparations are used intravenously to treat or prevent bleeding episodes in patients with hemophilia B by temporarily replacing deficient or missing endogenous Factor IX[1][3][5][6].
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