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Plasma H

Control Plasma (pool of healthy donors) (Plasma N) according to TU 9398-004-0559541-2009

Plasma N is intended for daily in-laboratory control of the accuracy and reproducibility of the reagent-analyzer system when determining the following hemostasis parameters in normal and pathological areas:

  • Prothrombin according to Quick in % of the norm; prothrombin index, %; prothrombin time (International Normalized Ratio, INR);
  • Thrombin time, sec;
  • Activated partial thromboplastin time (APTT), sec;
  • Fibrinogen content according to Clauss, g/L;
  • Antithrombin III (ATIII) activity, %;
  • Total fibrinolysis system (XIIa-dependent fibrinolysis), min.

Plasma N is designed to work both manually and on all types of semi-automatic and automatic coagulometers.

Method Principle: Plasma N is analyzed in one series of measurements with the test plasma when performing tests: prothrombin time, APTT, thrombin time, determination of fibrinogen concentration, determination of ATIII activity, and determination of the total fibrinolysis system according to the instructions provided with the corresponding reagent kits. The analyzed parameters of the control material should fall within the range of values specified in the kit's passport.

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The kit includes:

  • Human blood plasma with hemostasis parameters within normal limits, lyophilized (1 ml/vial) – 3 vials.
  • Human blood plasma with artificially reduced hemostasis parameters, lyophilized (1 ml/vial) – 3 vials.

The kit is intended for conducting 120 analyses, with a reagent consumption of 0.05 ml per analysis.