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Description
- Formulated in a proprietary purified protein matrix that mimics the composition of a true clinical specimen.Formulated in a Purified Protein Matrix that is fully commutable with true clinical specimens
- Can be used for verification of clinical assays, development of diagnostic tests and training of laboratory personnel
Specifications
Specifications
| Content And Storage | 2°C to 8°C |
| For Use With (Application) | Evaluating and monitoring of qualitative molecular diagnostic assays for the detection of Influenza A/B nucleic acid |
| Includes | 6 x 0.5 mL vials of NATtrolTM Influenza A and NATtrolTM Influenza B formulated in a Purified Protein Matrix that is fully commutable with true clinical specimens |
| Quantity | 6 x 0.5 mL |
This product is an IVD/CE marked USA FDA Class 1 exempt, unassayed external run control intended for in vitro diagnostic use and are for professional use only. NATtrol™ controls are not intended for use as a substitute for the internal controls provided by in vitro diagnostic kit manufacturers. Quality control materials should be used in accordance with local, state, federal and accreditation requirements.
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