Influenza A+B Rapid Test, in nasopharyngeal swab, throat swab or nasal aspirate specimens
A rapid test for the qualitative detection of Influenza A and Influenza B virus in nasal swab, throat swab or nasal aspirate specimens CE certified
Applications:
The Influenza A+B Rapid Test Dipstick is a rapid chromatographic immunoassay for the qualitative detection of influenza A and B antigens in nasal swab or throat swab or nasal aspirate specimens. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections.
Product features | Parameters |
Principle | Chromatographic Immunoassay |
Format | Dipstick, Cassette |
Specimen | Swab / Nasal Aspirate |
Certificate | CE |
Reading Time | 15 minutes |
Pack | 20T/25T |
Storage Temperature | 2-30°C |
Shelf Life | 2 Years |
Description:
Influenza (commonly known as ‘flu’) is a highly contagious, acute viral infection of the respiratory tract. It is a communicable disease easily transmitted through the coughing and sneezing of aerosolized droplets containing live virus.1 Influenza outbreaks occur each year during the fall and winter months. Type A viruses are typically more prevalent than type B viruses and are associated with most serious influenza epidemics, while type B infections are usually milder.
The gold standard of laboratory diagnosis is 14-day cell culture with one of a variety of cell lines that can support the growth of influenza virus.
Cell culture has limited clinical utility, as results are obtained too late in the clinical course for effective patient intervention. Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) is a newer method that is generally more sensitive than culture with improved detection rates over culture of 2-23%.3 However, RT-PCR is expensive, complex and must be performed in specialized laboratories.
The Influenza A+B Rapid Test Dipstick (Swab/Nasal Aspirate) qualitatively detects the presence of Influenza A and/or Influenza B antigen in nasal swab or throat swab or nasal aspirate specimens, providing results within 15 minutes. The test uses antibodies specific for Influenza A and Influenza B to selectively detect Influenza A and Influenza B antigen in nasal swab, throat swab or nasal aspirate specimens.
How to use?
INTERPRETATION OF RESULTS
(Please refer to the illustration above)
POSITIVE Influenza A:* Two distinct colored lines appear. One colored line should be in the control region (C) and another colored line should be in the Influenza A region (A). A positive result in the Influenza A region indicates that Influenza A antigen was detected in the sample.
POSITIVE Influenza B:* Two distinct colored lines appear. One colored line should be in the control region (C) and another colored line should be in the Influenza B region (B). A positive result in the Influenza B region indicates that Influenza B antigen was detected in the sample.
POSITIVE Influenza A and Influenza B:* Three distinct colored lines appear. One colored line should be in the control region (C) and two colored line should be in the Influenza A region (A) and Influenza B region (B). A positive result in the Influenza A region and Influenza B region indicates that Influenza A antigen and Influenza B antigen were detected in the sample.
*NOTE: The intensity of the color in the test line regions (A or B) will vary based on the amount of Flu A or B antigen present in the sample. So any shade of color in the test regions (A or B) should be considered positive.
NEGATIVE: One colored line appears in the control region (C). No apparent colored line appears in the test line regions (A or B).
INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test Dipstick. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
Cat. No. | Product | Specimen | Pack |
IINA-525 | Influenza A/B +H1N1 Combo Rapid Test Cassette | Swab | 10T |