Influenza A/B Antigen Rapid Test is a lateral flow immunoassay for the qualitative detection of Influenza A and B virus antigens in nasal swab specimens from individuals suspected of Flu A/B.
Parameter of COVID-19 Antigen/Influenza A+B Antigen Combo Rapid Test
CE, ISO 13485：2016
Carton Box, 1 test/kit, 5 tests/kit, 20 tests/kit, 25 tests/kit, 50 tests/kit
Fast. You can read the result within 5-10 minutes, faster than PCR test.
Simple. Easy to use and easy to get the specimen, no equipment required, no PCR lab required.
Convenient. Can be used in many places like station, airport, hospital, school and very convenient.
COVID-19 Antigen/Influenza A+B Antigen Combo Rapid Test is based on colloidal gold immunochromatography assay.
During the test, specimens and detection buffer are applied to the test cartridges. If there are SARS-CoV-2 nucleocapsid antigens or influenza A/B virus in the specimens, they will bind to colloidal gold-labeled antibodies against SARS-CoV-2 N protein or Influenza A and B virus antigens respectively on conjugation pad forming virus antigen-antibody-colloidal gold complexes (complex A for Flu A, complex B for Flu B and complex C for COVID-19 ).
During lateral flow, the complexes move along nitrocellulose membrane toward one end of the absorbent paper. When passing the COVID-19 test line TC (coated with another monoclonal antibody against SARS-CoV-2 N protein), the complex C is captured by capture antibody resulting in coloring on line TC; when passing the Influenza A test line TA (coated with another monoclonal antibody against Influenza A virus N protein), the complex A is captured by capture antibody resulting in coloring on line TA; when passing the Influenza B test line TB (coated with another monoclonal antibody against Influenza B virus N protein), the complex B is captured by capture antibody resulting in coloring on line TB; when passing the line C, residual colloidal gold-labeled control molecule is captured by quality-control antibody resulting in coloring on line C.
1. Test cartridge
2. Pre-filled extraction buffer tube
3. Nozzles to extraction tube
4. Nasal swab
5. Paper rack
1. Carefully insert the entire absorbent tip of the swab in one nostril and rotate at least 5 times. Be sure that the absorbent
tip of the swab scrapes against the nasal wall.
2. Remove swab from nostril and, using the same swab, repeat step 1 in the other nostril.
3. Insert the absorbent tip of the swab into the extraction buffer tube and swirl the swab at least 5 times.
4. Squeeze the tube against the submerged swab several times to facilitate extraction of the specimen. Remove the swab,
place it back in its original wrapping and dispose into the waste bag.
5. Place the nozzle onto the extraction tube and ensure it is attached firmly.
Restore the test devices and specimens to room temperature (15-30°C ) prior to testing.
1. Remove the cassette device from the sealed pouch just prior to testing. Lay the device on a clean, flat surface and label with
2. Invert the sample extraction tube and slowly add 2~3 drops of the extracted specimen into the sample well of the cassette device
by gently squeezing the sample tube.
3. Set the timing device for 15 minutes.
4. Read the results after 15 minutes. Note: The result might be visible after a shorter time, however, it should only be interpreted
between 15-20 minutes after dispensing the sample material onto the cassette device.
5. Collect all used items (swab, cassette, sample extraction tube, foil seal and nozzle, and potentially used gloves) into the waste bag.
Close the bag and dispose in a biohazard trash can.
6. Thoroughly wash or sanitize hands and any used surfaces/tools for the procedure.
1. Negative results: coloring on C line appear only.
2. Flu A positive results: coloring on both A line and C line. (Note: Faint line should be regard as coloring)
3. Flu B positive results: coloring on both B line and C line. (Note: Faint line should be regard as coloring)
4. Invalid results: no coloring appear on C line regardless of A and B line coloring.
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