Flu Verification Panel

ZeptoMetrix external controls have demonstrated performance on a variety of molecular assays. The product has been tested with the Luminex® VERIGENE®, Roche cobas®Liat®, or Abbott ID Now™ systems and provides the expected results, however performance characteristics must be established by the end user.

NATtrol Flu Verification Panel includes 6 targets: Influenza AH1 strain A/New Caledonia/20/99, Influenza AH3 strain A/Brisbane/10/07, Influenza A H1N1 strain A/NY/02/09*, Influenza B strain B/Florida/02/06, Respiratory Syncytial Virus A, and Respiratory Syncytial Virus B strain CH93(18)-18.

• Formulated with purified, intact organisms
• Organisms are chemically modified to render them noninfectious
• Refrigerator stable—store between 2 and 8°C
• Purified protein matrix treated with 0.09% sodium azide
• 7 x 0.5 mL vials

NATtrol products are ready-to-use, inactivated full process controls designed to evaluate performance of molecular tests. They can be used for verification of assays, training of laboratory personnel and to monitor assay-kit lot performance. NATtrol products contain intact organisms and should be run in a manner similar to clinical specimens.

NATtrol™ Flu Verification Panel is designed to evaluate the performance of nucleic acid tests for determination of the presence of viral nucleic acids (from organisms listed in Table 1). NATtrol™ Flu Verification Panel can also be used for validation of clinical assays, development of diagnostic tests and training of laboratory personnel.

• ENGLISH (PI)
• ENGLISH (SDS)

For Research Use Only. Not for use in diagnostic procedures. Quality control materials should be used in accordance with local, state, federal, and accreditation requirements. This product is not intended to replace the manufacturer's controls provided with the assay. Propagation or commercialization are prohibited without prior written consent from Antylia Scientific.

When used as a control for nucleic acid tests, the same protocols as those used to amplify extracted clinical specimens should be employed.

The suitability and performance characteristics should be determined by your laboratory for each intended usage.