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Vitamin K-dependent protein

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Protein C is a vitamin K-dependent serine protease that regulates blood coagulation by inactivating factors Va and VIIIa in the presence of calcium ions and phospholipids. Exerts a protective effect on the endothelial cell barrier function.

Below are the list of possible Vitamin K-dependent protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Vitamin K-dependent protein C

 Vitamin K-dependent protein C ELISA Kit
 Vitamin K-dependent protein C Recombinant
 Vitamin K-dependent protein C Antibody
Also known as Vitamin K-dependent protein C (Anticoagulant protein C) (Autoprothrombin IIA) (Blood coagulation factor XIV).
PROC: Protein C is a vitamin K-dependent serine protease that regulates blood coagulation by inactivating factors Va and VIIIa in the presence of calcium ions and phospholipids

Protein type: Apoptosis; EC 3.4.21.69; Protease

Cellular Component: endoplasmic re
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ticulum; extracellular space; Golgi apparatus

Molecular Function: peptidase activity; protein self-association; serine-type endopeptidase activity

Biological Process: blood coagulation; liver development; negative regulation of apoptosis; negative regulation of blood coagulation; negative regulation of coagulation; negative regulation of inflammatory response; proteolysis
 Proc ELISA Kit
 Proc Recombinant
 Proc Antibody
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Vitamin K-dependent protein S

 Vitamin K-dependent protein S ELISA Kit
 Vitamin K-dependent protein S Recombinant
 Vitamin K-dependent protein S Antibody
PROS1: Anticoagulant plasma protein; it is a cofactor to activated protein C in the degradation of coagulation factors Va and VIIIa. It helps to prevent coagulation and stimulating fibrinolysis. Defects in PROS1 are the cause of thrombophilia due to protein S deficiency, autosomal dominant (THPH5). A hemostatic disorder characterized by impaired regulation of blood coagulation and a tendency to re
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current venous thrombosis. However, many adults with heterozygous disease may be asymptomatic. Based on the plasma levels of total and free PROS1 antigen as well as the serine protease-activated protein C cofactor activity, three types of PROS1D have been described: type I, characterized by reduced total and free PROS1 antigen levels together with reduced anticoagulant activity; type III, in which only free PROS1 antigen and PROS1 activity levels are reduced; and the rare type II which is characterized by normal concentrations of both total and free PROS1 antigen, but low cofactor activity. Defects in PROS1 are the cause of thrombophilia due to protein S deficiency, autosomal recessive (THPH6). A very rare and severe hematologic disorder resulting in thrombosis and secondary hemorrhage usually beginning in early infancy. Some affected individuals develop neonatal purpura fulminans, multifocal thrombosis, or intracranial hemorrhage.

Protein type: Secreted; Secreted, signal peptide

Cellular Component: extracellular space; protein complex

Molecular Function: protein complex binding

Biological Process: negative regulation of coagulation; positive regulation of phagocytosis
 Pros1 ELISA Kit
 Pros1 Recombinant
 Pros1 Antibody
 Pros ELISA Kit
 Pros Recombinant
 Pros Antibody
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Vitamin K-dependent protein Z

 Vitamin K-dependent protein Z ELISA Kit
 Vitamin K-dependent protein Z Recombinant
 Vitamin K-dependent protein Z Antibody
Inhibits activity of the coagulation protease factor Xa in the presence of SERPINA10, calcium and phospholipids (). Appears to assist hemostasis by binding thrombin and promoting its association with phospholipid vesicles.
 PROZ ELISA Kit
 PROZ Recombinant
 PROZ Antibody
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