» Factor IX Inhibitor Plasma Negative Control

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

Factor IX Inhibitor Plasma Negative Control

Nijmegen Bethesda Controls

Factor IX deficient plasmas without Factor IX inhibitor.
This plasma can be used for the negative control of the determination of Factor IX (FIX) inhibitor according to the Bethesda assays or modified Nijmegen Bethesda assays.

Factor IX Inhibitor Plasma Negative Control is made from a pool of Factor IX deficient (<1%) human plasma.
It does not contain any specific natural inhibitor directed against the activity of Factor IX (FIX).

Reference	6-1950-05
Presentation	Vial
Format	25 x 0.5 mL
Quote

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

Reference	Presentation	Format	Quote	Product sheet
6-1950-05	Vial	25 x 0.5 mL

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

Factor IX Inhibitor Plasma Negative Control Certificate of analysis

Treatment for hemophilia B involves injecting the missing Factor IX I.V. to prevent or stop bleeding.
A majority of the complications of this treatment are the development of antibodies against FIX, called inhibitors.
The development of an anti-FIX 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 FIX for hemophilia B.

- 25 cryotubes x 0.5 mL of frozen plasma

CRYOcheck™ Factor VIII Inhibitor Kit
Factor IX Inhibitor Plasma Weak Control
Factor VIII Inhibitor Plasma
Factor VIII Inhibitor Plasma HCV neg
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 FIX INHIBITOR NIJMEGEN BETHESDA CONTROLS