Influenza Verification Panel (18 x 0.5mL)

NATtrol Influenza Verification Panel (qualitative) is formulated with purified, intact viral particles that have been chemically modified to render them non-infectious and refrigerator stable. NATFVP(XP)-C contains 18 x 0.5 mL vials of viral NATtrol as listed in Table 1 (3 x 0.5 mL vials each of Influenza A H1 and Influenza A H3, 6 x 0.5 mL vials of Influenza B and 6 x 0.5 mL vials of the Coxsackievirus A9 negative control). The panel members are supplied in a proprietary matrix.

NATtrol Influenza 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 Influenza Verification Panel can also be used for validation of clinical assays, development of diagnostic tests and training of laboratory personnel.

• ENGLISH (SDS)
• ENGLISH (PI)

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.

• Qualitative results are shown in Table 1 below.
• Each laboratory must evaluate the product and establish its own acceptance criteria.
• The table shown below is for informational purposes only.