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Factor VIIa
| Catalog | Product Name | EC No. | CAS No. | Source | Price |
|---|---|---|---|---|---|
| NATE-0884 | Native Human Factor VIIa | Human | Inquiry |
Related Reading
Factor VIIa plays a key role in the coagulation cascade, contributing to the formation of blood clots and the regulation of hemostasis. In this assay, we will explore the structure, function, application and clinical significance of factor VIIa and elucidate its importance in various physiological processes and therapeutic interventions.
Structure
Factor VIIa is a serine protease belonging to a family of vitamin K-dependent coagulation factors. Structurally, it consists of a heavy chain and a light chain, linked by disulfide bonds. The active site of factor VIIa includes the catalytic triad, consisting of His193, Asp348 and Ser195 residues, giving it proteolytic activity.
Functions
Factor VIIa acts as an activated form of Factor VII and, together with tissue factor (TF), initiates the extrinsic pathway of the coagulation cascade. Upon binding to TF, factor VIIa forms a complex that activates factors IX and X, leading to the conversion of prothrombin to thrombin. Thrombin in turn converts fibrinogen to fibrin, resulting in the formation of a stable blood clot.
Applications
- Hemophilia Treatment: Factor VIIa can be used to treat bleeding events in patients with hemophilia A or B who are deficient in factor VIII or IX, respectively. recombinant factor VIIa (rFVIIa) is used to promote clot formation and control bleeding, especially in cases of severe bleeding or when conventional therapies have failed.
- Surgical interventions: Factor VIIa may be used during surgical procedures where excessive bleeding poses a risk to the patient. by promoting hemostasis, Factor VIIa helps control bleeding and reduces the need for blood transfusions, thereby improving patient prognosis.
- Trauma management: Factor VIIa has been used as an adjunct to hemostatic therapy in the setting of trauma-related coagulopathies. It has the potential to improve clot formation, prevent uncontrolled bleeding, and support resuscitation efforts in severely injured patients.
- Inherited bleeding disorders: In addition to hemophilia, factor VIIa may be used in other rare bleeding disorders, such as factor VII deficiency. The use of rFVIIa in these patients can help normalize coagulation and prevent excessive bleeding.
Clinical significance
- Coagulation disorders: Mutations or deletions in the factor VII gene can lead to bleeding disorders. Identification of such genetic variants is important for the diagnosis and management of patients with abnormal coagulation, allowing for targeted therapeutic interventions.
- Thrombotic events: In some cases, increased levels of factor VIIa may lead to an increased risk of thrombotic events, such as deep vein thrombosis or arterial occlusion. Monitoring factor VIIa levels and considering their role in thrombotic risk assessment can help in patient management and prevention strategies.
- Research and development: Factor VIIa is an important research tool for studying the coagulation cascade and its associated disorders. Studying its mechanism of action and interactions with other coagulation factors can contribute to the understanding and treatment of various coagulation-related diseases.
Conclusion
Factor VIIa plays an important role in the initiation of the coagulation cascade, contributing to the formation of blood clots and the maintenance of hemostasis. Its structure, function and applications, particularly in the management of bleeding disorders and surgical interventions, highlight its clinical significance. Understanding the role and regulation of factor VIIa can help develop targeted therapies and diagnostics, improve patient outcomes, and advance our understanding of hemostasis-related disorders.