Labile Factor Accelerator globulin

Stable Factor Serum prothrombin conversion accelerator

Labile Factor Accelerator globulin

Stable Factor Serum prothrombin conversion accelerator

Labile Factor Accelerator globulin

Antihemophilic Factor globulin Antihemophilic factor A Platelet Co-factor1

Christmas Factor Component Antihemophilic Factor B Platelet co-factor2

Antihemophilic Factor globulin Antihemophilic factor A Platelet Co-factor1

Stuart factor Prower factor Autoprothrombin III

Plasma thromboplastin antecedent

Antihemophilic factor C antecedent

Plasma thromboplastin antecedent

Antihemophilic factor C antecedent

Laki-Lorand Fibrinase Plasma transglutaminase Fibrinoligase

Factor Contact activation co-factor Williams Factor Flaujeac Factor

F VIII: Coagulant Factor T Function

A cofactor for the activation of the intrinsic pathway

Hemophilia A: Factor 8 Deficiency

In Hemophilia A, the defective is the coagulant T factor 8

Defective Factor VIII:C

Hemophilia A: Factor 8 Deficiency

In Hemophilia A, the defective is the coagulant T factor 8

A cofactor for the activation of the intrinsic pathway

Hemostatic Function: Substrate

CF V, VIII, HMWK, Factor 4 - Ca+2

Serine Protease - ( Factor II, VII, IX, XI, XII, PK)

Hemostatic Function: Co Factor

CF V, VIII, HMWK, Factor 4 - Ca+2

Serine Protease - ( Factor II, VII, IX, XI, XII, PK)

Hemostatic Function: Enzyme

Serine Protease - ( Factor II, VII, IX, XI, XII, PK)

Transaminase - Factor XIII: Fibrin Stabilizing Clotting Factor

CF V, VIII, HMWK, Factor 4 - Ca+2

Physical Properties: Present in stored plasma/ aged plasma: YES

Fibrinogen Group (Except 5 and 8)

Secondary Hemostasis

Authored by JM Gorospe

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5 sec • 1 pt