Respiratory Verification Panel (15 x 0.5mL; 2 x 1mL)
- Volume: 1.0mL
- Units/Pack: 17
- Storage Condition: 2-8°C
- Hazardous Information: Non-Infectious
- Matrix: Purified protein matrix treated with 0.09% sodium azide
- Product Type: Panel
For Research Use Only. Not for use in Diagnostic Procedures.
ZeptoMetrix external controls have demonstrated performance on a variety of molecular assays. The product has been tested with the Luminex® VERIGENE® system and provides the expected results, however performance characteristics must be established by the end user.
NATtrol Respiratory Verification Panel includes 15 targets: Influenza B strain B/Florida/02/06, RSV A, RSV B strain CH93(18)-18, Parainfluenza 1, Parainfluenza 2, hMPV-8 strain Peru6-2003, Adenovirus 3, Influenza A H1 strain A/Singapore/63/04, Influenza A H3N2 strain A/Brisbane/10/07, Parainfluenza 3, Parainfluenza 4, Rhinovirus 1A, B. holmesii strain F061, B. pertussis strain A639, and B. parapertussis strain A747.
- 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
- 15 x 0.5 mL vials of bacterial or viral targets and 2 x 1.0 mL vials of negative control
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.
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.