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Covid-19 Antigen Rapid Test Kit

SARS-CoV-2 Nasal & Oral ​Antigen Detection Kits

This rapid antigen test kit is for the qualitative detection of SARS-CoV-2 specific antigens currently present in the human nasopharyn & oropharynx by the reliable, rapid colloidial gold method.

KEY FEATURES:
* Both Symptomatic & Asymptomatic Individuals are detectable
* Easy to Use & Read
* Quick Result
* Highly Sensitive and Specificity
* No Specific Training
* No Instrument required
* Convenient for Self Testing
MANUFACTURE: TECBOD

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SARS-CoV-2 Nasal & Oral Antigen Detection Kits

This coronavirus antigen test kit is a lateral flow immunisation for the qualitative detection of SARS-COV-2 antigen (nucleoside protein) in upper respiratory samples with nasal swabs or saliva during the acute phase of infection. With the properties of fast, accurate, easy to use and reliable. For in vitriol diagnostic use only and self-testing.

SPECIFICATION:

Assay Format: Lateral flow test / Immunochromatographic
Testing Result: In 10-15 minutes
Sensitivity: 94.25% (95% CI:87.10%-98.11%)
Specificity: 100% (95% CI:96.97%-100.00%)
Total agreement: 97.58% (95% CI:87.75%-95.52%)
Specimen Collection: nasopharyngeal / oropharyngeal Swab
INSIDE THE PACKAGE:
1. Sterile Swab * 1
2. Antigen Extraction Tube
3. Antigen Extract R1
4. Test Card
STORAGE & VALIDITY:
* Store at 4℃~30℃, and it is valid for 24 months.
* After the aluminum foil bag is unsealed, the test card should be used as soon as possible within one hour.
SPECIMEN COLLECTION:
1.Throat swab: Let the patient's head tilt slightly, mouth open, and make "ah" sounds, exposing the pharyngeal tonsils on both sides. Hold the swab and wipe the pharyngeal tonsils on both sides of the patient with a little hard back and forth at least 3 times; place the swab specimen in the Antigen extraction tube with the Antigen extract R1 added in advance, rotate the swab for about 10 seconds, and press the swab head against the wall to release the antigen in the swab.
2.Nasal swab: Let the patient's head relax naturally, and slowly rotate the swab against the wall of the nostril into the patient's nostril to the nasal palate, and then slowly remove it while wiping. Using the same swab, wipe the other nostril in the same way; place the swab specimen in the Antigen extraction tube with the Antigen extract R1 added in advance, rotate the swab for about 10 seconds, and press the swab head against the wall to release the antigen in the swab.
PERFORMING A TEST:
The test method was colloidal gold. Please read the manual and the instrument operation manual carefully before use.
1. Open the package, take out the test card and place it on a clean and stable surface.
2. After collecting the swab sample with the sterile swab provided, unscrew the bottle cap ① of the Antigen extraction tube bottle that contains the Antigen extract R1 and insert the sample swab.
3. Put the swab specimen into the Antigen extraction tube, rotate the swab for about 10 seconds, and press the swab head against the tube wall to release the antigen in the swab. Squeeze the swab over the head to remove the swab so as to remove as much liquid as possible from the swab. Dispose of swabs according to biohazard waste disposal method.
4. Screw the bottle cap ① on the Antigen extraction tube.
5.Unscrew the bottle cap ② and put 2 drops into the specimen hole of the test card, and start the timer.
6.Read the results within 10-15 minutes. Strong positive results can be reported within 15 minutes, however, negative results must be reported after 15 minutes, and the results after 30 minutes are no longer valid.



INTERPRETATION OF THE TEST RESULT






Negative Posative Invalid
FAQ

Q: How accurate is antigen rapid test kit?
A: For rapid antigen tests, this includes a clinical sensitivity of at least 80% (for specimens collected within 7 days of symptom onset) and a clinical specificity of at least 98%.
Q: Is there a difference between rapid antigen and antigen test?
A: The rapid test is less accurate and there is a greater chance for a false negative. Plus, the test will only pick up if the virus is active in your body, meaning asymptomatic cases – when someone doesn't have any symptoms – are harder to identify with the antigen test.
Q: What is a PCR test?
A: The PCR test takes a sample of ribonucleic acid (RNA) and “amplifies” it with the help of lab technologies. Amplifying RNA helps to make even small traces of the COVID-19 virus visible in the test sample. Even if you have a small trace of the virus in your system, the PCR test will detect it.
The PCR test doesn’t alter your genetic material – DNA – in any way, and your test provider isn’t able to do anything with your DNA besides tell if you’re positive with COVID-19.
Q: What is a antigen test?
A: The rapid test, called an antigen test, checks for proteins that are found on the outside of the virus.
The antigen test mimics what antibodies do. Antibodies are the “good guys” that attach to the antigen protein (the “bad guys”) and fight the virus. When you give your nasal swab sample, it’s put into a liquid and then onto a test strip.
The test strip acts like an antibody – if there are any COVID-19 antigen “bad guys” in your system, the molecules in the liquid will attach to those antigens, and a line will appear on the test strip. This means you’re positive for COVID-19. If there are no antigens detected in your system, the liquid doesn’t respond and no line will appear, often meaning you are negative for the virus.
Q: Can at-home COVID-19 tests detect Omicron?
A: The answer is yes. Although rapid antigen tests might have reduced sensitivity at detecting the omicron variant.The omicron variant has some mutation-related changes in the nucleocapsid protein, which is the target that most at-home antigen tests are designed to detect.
Q: Which is better RT-PCR or antigen?
A: Although it is less sensitive than the RT-PCR test, the antigen test is an effective way to monitor infection in people who are in close contact with COVID-19 infected. Rapid antigen tests are often used as mass screening tests to detect SARS-CoV-2 infection quickly in containment zones or healthcare settings.

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