Influenza Rapid Test Validation Panel 1 (RUO)

NAME AND INTENDED USE:
The Influenza Rapid Test Verification Panel I is intended for use with in vitro assay procedures to determine the absence or presence of Influenza. This panel is for Research Use Only and should not be used in diagnostic procedures.

SUMMARY:
The Influenza Rapid Test Verification Panel I is composed of twenty members representing various influenza strains and a range of reactivities. Each panel member contains 0.5mL of material prepared from inactivated viral culture fluid. This panel can be used for training, lot-to-lot comparison of reagent test kits and to evaluate and compare intra laboratory and inter laboratory performance of Influenza testing platforms.

PRINCIPLES OF THE PROCEDURE:
The Influenza Rapid Test Verification Panel I reagents have been designed for use with in vitro assay procedures for monitoring assay performance across a range of reactivity levels. These materials are prepared from inactivated viral culture fluids. Source materials have been processed and treated to eliminate unwanted components and to ensure stability of the final product. The Influenza Rapid Test Verification Panel I members should be evaluated as an unknown specimen per the instructions supplied by the manufacturer of the test kit being used.

REAGENTS:
1. Eight vials Influenza A/B Non-Reactive (0.5mL each).
2. Seven vials Influenza A Reactive (0.5mL each).
3. Five vials Influenza B Reactive (0.5mL each).

For Research Use Only.

Product Information