2019 Ag Rapid Test Kit Neutralizing Antibody Rapid Test Method Vaccination

Sample Requirements

1. Collect serum, plasma or whole blood samples.
2. Sediment and plankton in the sample will affect the experimental results, so it needs to be removed by centrifugation.
3. Anti-coagulation therapy: loofah anti-coagulation therapy, EDA anti-coagulation therapy, sodium citrate anti-coagulation therapy has no obvious effect.
4. Blood collection by experts is needed. Serum/serum/plasma tests are recommended. In emergency or special circumstances, a patient's whole blood sample can also be used for rapid testing.
5. Serum and plasma samples should not be stored for more than 8 hours at room temperature.
It can be stored for 5 days at 2-8 ℃ and 6 months below -20℃, but please avoid repeated freezing and melting. Whole blood samples do not freeze and need to be stored at 2℃ to 8℃ for 48 hours.

Test Method

Please read the instructions carefully before testing. Before the test, all reagents should be returned to room temperature and tests must be carried out at room temperature.
1. Take the test card out of the box and use it within 1 hour.
2. Add 20L sample (serum, plasma or whole blood) and 2 drops (~ 60L) of sample buffer storage into the filling hole of the test card, and start timing.
3. After 10 to 15 minutes of reaction at room temperature, read the results. Invalid after 20 minutes.

Interpretation of Test Results

 Test card description:
1. Invalid result: Quality management line (Line C) is invalid and needs to be tested again.
2. Negative result: The appearance color of test line (T line) is above the reference line (R line), quality management line (C line) and reference line (R line).
3. Positive results: the test line (T line) or the red watchband is not displayed on the red watchband, the test line (T line) is lower than the reference line (R line), quality management line (C) and the reference line (R line) with color.

Limitation of Test Method

This kit is for qualitative analysis and INVitro diagnostics only.
2. Please add appropriate test samples. With too many or too few samples, the results may be incorrect.
3. Hemolysis, lipids in the blood, jaundice and sample contamination may affect the test results, so please try to avoid them.
4. The test results of the reagent are for clinical reference only, and should not be used as the sole basis for clinical diagnosis and treatment. The final diagnosis of the disease is made by combining all clinical and examination results.

Precautions

1. This product is only used for Invitro diagnosis.
This product is disposable and can't be reused.
3. Please read the instructions carefully before operation, and strictly follow the instructions of reagent for experimental operation.
4. Please avoid conducting the experiment under harsh environmental conditions (84 disinfectants, sodium hypochlorite, acid, alkali, acetaldehyde, other corrosive gases with high concentration, dust, etc.). Laboratory disinfection needs to be carried out after the experiment.
5. All samples and reagents used shall be considered as potentially infectious substances and shall be disposed of in accordance with local regulations.
6. The reagent must be used within the expiry date stated on the package. To prevent moisture, the test card needs to be removed from the aluminum foil bag as soon as possible after removal.

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