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.
Human deficient plasma for the determination of Factor XII.
Reference
Presentation
Packaging
6-PPD12-ID
Vial
1 x 1.0 mL
The Safety Data Sheets and Notices are accessible to our registered customers.
Factor XII (FXII) is a glycoprotein synthesized by the liver. FXII participates in the contact phase which initiates the intrinsic pathway of coagulation.
Activated on contact with a negatively charged surface, it becomes capable of activating prekallikrein and kallikrein (amplified by KHPM) then FXI to FXIa in the presence of KHPM.
The FXIa thus formed activates the FXII in FXIIa, amplifying the reaction.
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.
Plastic bottles.
Reduces the time needed to set up your test protocols.
Ready to use after thawing.
