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.
Low D-Dimer control plasmas
300 ng / mL control plasmas used for the Technoleia® D-Dimer Latex kit assay kit.
5 x 1.0 mL
The Safety Data Sheets and Notices are accessible to our registered customers.
D-Dimers are fragments resulting from the destruction of fibrin during fibrinolysis.
A low level of D-Dimer is normal and indicates that there has been activation of the coagulation and formation of a clot, but can strongly increase in the event of venous thrombosis, DIC (disseminated intravascular coagulation) or pulmonary embolism.
The Technoleia® D-Dimer test comprises an anti-D-Dimer monoclonal antibody coupled to the latex microparticles and forms a high molecular weight complex with the D-Dimer in the sample.
This results in a photometrically detectable change in turbidimetry of the sample which is directly proportional to the concentration of antigens within the sample.
Controls should be treated the same as patient plasmas.
The remaining calibrators and controls can be aliquoted and frozen.