FVIII:C Deficient Plasma (6 x 1 mL)
For In Vitro Diagnostic Use.
In EU: This Product is CE Marked.
Health Canada Licensed
Deficient plasma for the assay of Factor VIII:C. All the clotting factors are present (constant and in the normal range, brought by the deficient plasma), except for FVIII:C, which is brought by the diluted tested plasma, and clotting is triggered with cephalin, activator and calcium (APTT). FVIII:C is the limiting factor and clotting time is inversely proportional to the concentration of FVIII:C.
For measurement of Factor VIII:C (FVIII:C) activity.
For any in vitro protocol or research study where a source of human FVIII:C deficient plasma is required.
Associated calibrator and controls are available: BIOPHEN Plasma Calibrator (Ref A222101-CAN), BIOPHEN Normal Control Plasma (Ref A223201-CAN) and BIOPHEN Abnormal Control Plasma (Ref A223301-CAN).
Please Note: IVD Not for Sale in US. For US availability CLICK HERE.
Instructions For Use
Material Safety Data Sheet (MSDS)
Certificate of Analysis (COA)