» Fibrinogen Reagent Kit

ROUTINE SCREENING TESTS FIBRINOGEN

Fibrinogen Reagent Kit

Chronometric assay

Fibrinogen assay based on the (modified) Clauss method.

For this routine hemostasis test, the clotting time of the diluted citrated plasma is determined in the presence of excess thrombin (≈ 80 IU / mL) and a reaction accelerator.

Reference	Presentation	Number of tests
4-5138005	Kit	45

The Safety Data Sheets and Notices are accessible to our registered customers.

Fibrinogen is a soluble protein made by the liver. Under the action of thrombin, fibrinogen is converted into fibrin. In association with FXIII, calcium ions, fibrin forms a stable network which ensures coagulation.

A linear relationship exists between the logarithm of the clotting time and the logarithm of the concentration of fibrinogen. The kit reference 4-5138005 is composed of 5 vials of 2 mL of reagent and a vial for calibration.

Linearity from 0.6 to 7 g / L
Stable 5 days in analyzers
No interference for :
- Heparin : UFH: ≤ 2 IU / mL -> CBrN
- Fibrinogen fragment ≤ 500mg / dL
- Bilirubin : ≤ 0.4 mg / dL

5 vials x 2 mL lyophilized reagent
1 vial x 1 mL of Coagulation Reference

Coagulation Control A
Coagulation Control N
Coagulation Reference
TECHNOCLOT® Control A
TECHNOCLOT® Control N

	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.

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ROUTINE SCREENING TESTS FIBRINOGEN