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 deficient for Factor VII assay.
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from 50 mL
The Safety Data Sheets and Notices are accessible to our registered customers.
Factor VII (FVII) is a glycoprotein synthesized by the liver, vitamin k dependent. When tissue factor (TF) appears on the surface of damaged, abnormal or activated vascular endothelium, FVIIa associates with it, initiating the extrinsic pathway of coagulation.
The FT-FVIIa complex activates the FX in FXa and the FIX in FIXa.
This plasma is immunodepleted and assayed at less than 1% for the specific factor.
Freezing the plasmas at -80 °C makes it possible to keep the matrix perfectly intact and to avoid reconstitution.
Our packages contain dry ice for transport.
No additives or preservatives.
Expiration date> 1 year.
Reduces the time needed to set up your test protocols.
Ready to use after thawing.