» Factor VIII Inhibitor Plasma

HEMOSTASIS COAGULATION ROUTINE INHIBITOR NIJMEGEN BETHESDA ASSAYS FVIII INHIBITOR NIJMEGEN BETHESDA CONTROLS

Factor VIII Inhibitor Plasma

Lyophilized plasmas

Human hemophilia A plasma containing a natural anti-FVIII inhibitor.
This plasma can be used for the control of the determination of Factor VIII (FVIII) inhibitor according to the Bethesda assays or modified Nijmegen Bethesda assays.

Factor VIII Inhibitor control plasma is human hemophilia A plasma containing a specific natural antibody directed against FVIII (FVIII: C) activity.

Access on the manufacturer's website TECHNOCLONE

Reference	4-5159008
Presentation	Vial
Format	5 x 1.0 mL
Quote

Price list, safety data sheets and notices are accessible to our registered customers.

Reference	Presentation	Format	Quote	Product sheet
4-5159008	Vial	5 x 1.0 mL

Price list, safety data sheets and notices are accessible to our registered customers.

Treatment for hemophilia A consists of injecting the missing Factor VIII by I.V. to prevent or stop the bleeding. A majority of the complications of this treatment are the development of antibodies against FVIII, called inhibitors.

The development of an anti-FVIII inhibitor leads to episodes of bleeding that are difficult to control.
The activity of the inhibitor is measured by the Bethesda assays or modified Nijmegen Bethesda and is expressed in BU. 1BU neutralizes 50% of the activity of FVIII for hemophilia A.

Plasma with Factor VIII inhibitor can be used :

- As a plasma sample from a patient with hemophilia A with a Factor VIII inhibitor
- For accuracy control of Factor VIII inhibitor determination based on the Bethesda Test
- Title in Bethesda Unit depending on lots and tests
- 1 month stability after reconstitution

- 5 vials x 1 mL lyophilized plasma

CRYOcheck™ Factor VIII Inhibitor Kit
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Factor VIII Inhibitor Plasma Negative Control
Factor VIII Inhibitor Plasma Weak Control

	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.
	Manufacturer.
	Importer
	Distributor.

HEMOSTASIS COAGULATION ROUTINE INHIBITOR NIJMEGEN BETHESDA ASSAYS FVIII INHIBITOR NIJMEGEN BETHESDA CONTROLS