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 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.
Biological risk products.
Storage between 2 and 8 ° C.
Reactive in liquid form.
Reactive in lyophilized form.
Reactive in frozen form.
Stability after opening at 2-8 ° C.
Products that can be refrozen.
Stability 12 months after refreezing at -20 ° C.
Plasma for the determination of thrombin time (TT).
Standardized reagent for the determination of thrombin time.
6 x 6.0 mL
The Safety Data Sheets and Notices are accessible to our registered customers.
Thrombin time measurement is the time it takes for a fibrin clot to form after reagent addition, results are reported in seconds. If the clotting time of a sample is prolonged beyond the reference range, the level or activity of fibrinogen is low or thrombin inhibitors may be present.
Thrombin time is used :
- to qualitatively detect fibrinogen abnormalities.
- to assess the effectiveness of fibrinolytic treatment.
This reagent is standardized for the time of thrombin produced from bovine thrombin for the normal and therapeutic ranges (heparin and fibrinolytic).
- Adaptable to analyzer
- Allows a large number of tests to be carried out