Quick and Easy Influenza Ag A Test Nasopharyngeal Swab Results in 5min Suitable for 4-30C Environment

                                                      Influenza Ag A Test (Nasopharyngeal Swab)

FOR PROFESSIONAL IN VITRO DIAGNOSTIC USE ONLY Intended Us

e The Influenza Ag A Test is a rapid chromatographic immunoassay for the qualitative detection of influenza A virus antigen in nasopharyngeal swab specimens. Summar

y The Influenza Ag A Test is a rapid chromatographic immunoassay for the qualitative detection of influenza A antigen in nasopharyngeal swab specimens from individuals with suspected influenza A infection in conjunction with clinical presentation and the results of other laboratory tests. Results are for the detection of influenza A antigen. An antigen is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results indicate the presence of viral antigen, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out other bacterial/viral infection. The agent detected may not be the definite cause of disease. Negative results do not preclude influenza A infection and should not be used as the sole basis for treatment or patient management decisions. Negative results should be treated as presumptive and confirmed with a molecular assay, if necessary for patient management. Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with influenza A virus. The Influenza Ag A Test is intended for use by trained clinical laboratory personne. Principle

The Influenza Ag A Test is a qualitative, lateral flow immunoassay for the detection of influenza A nucleoproteins in nasopharyngeal swab specimens. In this test, antibody specific to the influenza A nucleoproteins is separately coated on the test line regions of the test strip. During testing, the extracted specimen reacts with the antibody to influenza A that is coated onto particles. The mixture migrates up the membrane to react with the antibody to influenza A on the membrane and generate a colored line in the test regions. The presence of this colored line in the test region indicates a positive result. To serve as a procedural control, a colored line will always appear in the control region if the test has performed properly.

 Precautions

1. For professional in vitro diagnostic use only. Do not use after expiration date. 2. Do not eat, drink or smoke in the area where the specimens and kits are handled. 3. Handle all specimens as if they contain infectious agents. 4. Observe established precautions against microbiological hazards throughout all procedures and follow the standard procedures for proper disposal of specimens. 5. Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed. 6. Follow standard biosafety guidelines for handling and disposal of potential infective material. 7. Humidity and temperature can adversely affect results.