Influenza A H1 Stock (Quantitative) (1 mL) -  Log in for Price

Influenza A H1 Stock (1mL)

Product Information:
    • Volume: 1.0mL
    • Units/Pack: 1
    • Storage Condition: 2-8°C
    • Hazardous Information: Non-Infectious
    • Matrix: Purified protein matrix treated with 0.09% sodium azide
    • Target: 1,000,000 copies/mL
    • Product Type: Inactivated Organism
  • Classification/ Permits:
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    For Research Use Only. Not for use in Diagnostic Procedures.


ZeptoMetrix external quality controls and verification panels, have demonstrated performance on a variety of molecular platforms. Based upon the platform and assay’s product configuration, including but not limited to fill volumes and concentrations of analytes, we recommend our NATtrol Influenza A H1 Stock 1mL Virus Stock (quantitative) to be used in conjunction with a real-time PCR thermal cycler.

  • 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
  • NATtrol Influenza A H1 Stock 1mL is quantitative
  • 1 mL vial
  • Target concentration of 1,000,000 copies/mL


NATtrol™ Influenza A H1 stock is designed to evaluate the performance of nucleic acid tests for the determination of the presence of Influenza A H1 Virus nucleic acid. NATtrol™ Influenza A H1 stock enables laboratories to monitor test variation, lot-to-lot test kit performance, and operator variation and can provide assistance in identifying random or systematic error

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.

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