BIOPHEN Arixtra® Control Plasma
In CE: This Product is CE Marked.
Health Canada Licensed.
Quality control plasmas (2 different levels at about 0.40 and 1.20 µg/mL) for the quality control of Arixtra® (Fondaparinux) testing using anti-Xa colorimetric assays.
|SKU ID#||Packaging||Website Links|
|A224001-RUO||2x6x1 mL||www.calibrators-controls.com |
|Assay Characteristics||Kit Components||Applications|
Normal human plasmas supplemented with Arixtra® at various levels.
Concentrations are established against a reference preparation for Arixtra®.
High stability following reconstitution.
|12 vials of 1 mL of human plasma supplemented at 2 different concentrations of Arixtra® (6 vials for each concentration).||Quality control of Arixtra® testing (BIOPHEN Heparin). |
Specific for Arixtra®.
Please note: This product is intended for Research Use Only (RUO) in the US, and must bear RUO labeling per FDA regulations. Alternate CE Mark (IVD) labeling for use in countries outside the US is available below.
Streamline Laboratory ProceduresReady-to-use reagents and buffers, from Medicago AB. Available in tablets and pouches.
|Package Inserts||MSDS||Tech Specs||Adaptations|
|BIOPHEN Arixtra® Cont Plas - RUO|
BIOPHEN Arixtra® Cont Plas - CE
|BIOPHEN Arixtra® Cont Plas||BIOPHEN Arixtra® Cont Plas||N/A|