Coagulation is the process of formation of a fibrin clot that begins almost instantly after an injury to the blood vessel has damaged the endothelium. The coagulation cascade has two pathways, the intrinsic pathway (also known as the contact activation pathway), and the extrinsic pathway (also known as the tissue factor pathway), which lead to fibrin formation.
Sino Biological offers a comprehensive set of tools for study of the coagulation cascade, including recombinant proteins, antibodies (rabbit MAbs, mouse MAbs, rabbit PAbs), ELISA kits, and gene cDNA clones.
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Coagulation is the process of formation of a fibrin clot. Coagulation is an important part of hemostasis, the process of blood clotting and then the subsequent dissolution of the clot, following repair of the injured tissue. Coagulation begins almost instantly after an injury to the blood vessel has damaged the endothelium. When the endothelium is damaged, the von Willebrand factor (vWF) is exposed to blood and recruits Factor VIII, collagen, and other coagulation factors. Circulating platelets adhere to exposed collagen, release the contents of their granules, and aggregate at the site of injury, forming a temporary, loose platelet plug. To insure stability of the initially loose platelet plug, proteins in the blood plasma, called coagulation factors or clotting factors, respond in a complex cascade to form fibrin clots.
The coagulation cascade has two pathways, the intrinsic pathway (also known as the contact activation pathway), and the extrinsic pathway (also known as the tissue factor pathway), which lead to fibrin formation. Although they are initiated by distinct mechanisms, the two converge on a common pathway that leads to clot formation. Both pathways are complex and involve numerous different proteins termed coagulation factors. The coagulation factors circulate as inactive zymogens. In the coagulation cascade, a zymogen of a serine protease and its glycoprotein co-factor are activated to become active components that then catalyze the next reaction in the cascade, ultimately resulting in cross-linked fibrin.
The coagulation system overlaps with the immune system. Coagulation can physically trap invading microbes in blood clots. Also, some products of the coagulation system can contribute to the innate immune system by their ability to increase vascular permeability and act as chemotactic agents for phagocytic cells. In addition, some of the products of the coagulation system are directly antimicrobial. Disorders of coagulation can lead to an increased risk of bleeding (hemorrhage) or clotting (thrombosis). Hemophilias include hemophilia A (coagulation factor VIII deficiency), hemophilia B (coagulation factor IX deficiency), hemophilia C (coagulation factor XI deficiency), hypofibrinogenemia, von Willebrand disease (vWD), and more. Thrombosis is the pathological development of blood clots, which become mobile and migrate to another part of the body, interfering with blood circulation and hence impairing organ function downstream of the occlusion.