Prekallikrein is a vitamin K-dependent glycoprotein non-covalently complexed with high molecular weight kininogen. It participates in the activation of coagulation depending on the surface, in fibrinolysis, in the generation of kinins and in inflammatory phenomena.
The prekallikrein deficits prolong the activated partial thromboplastin time (TCA), which varies according to the reagents (significant lengthening with silica or kaolin), without modification of the other coagulation tests.
The TCA can be corrected by adding control plasma and in the absence of deficiency in FVIII, FIX, FXI, FXII.
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These kits are manufactured in accordance with the 98/79 EC directive for in vitro diagnostic devices. Only CE marked products can be used for diagnostic applications in Europe.
These kits are intended for in vitro diagnostic use.
These kits are intended for in vitro diagnostic use.
These kits are for research use only and are not intended to be used for diagnostic procedures.
Federal Drug Administration, FDA validates diagnostic kits for in vitro diagnostic use in the United States.