2019 Ag Rapid Test Kit Neutralizing Antibody Rapid Test Sample Buffer

The storage temperature is 2℃ ~ 30℃, and the validity period is 12 months.
Aluminum foil bags are valid for 1 hour.
Production Lot Number: Refer to the label for details.
Expiry date: Please see the label for details.

Sample Requirements

1. Serum, plasma or whole blood samples were collected.
2. Sediment and plankton in the sample will affect the experimental results, so it needs to be removed by centrifugation.
3. Anti-coagulant: luffa anti-coagulant, EDA anti-coagulant, sodium citrate anti-coagulant effect is not obvious.
4. Blood collection by experts is needed. Serum/serum/plasma tests are recommended. A patient's whole blood sample can also be used for rapid testing in emergency or exceptional circumstances.
5. Serum and plasma samples should not be stored for more than 8 hours at room temperature.
2 ~ 8°C within 5 days, less than -20°C can be stored for 6 months, but please avoid repeated freezing melting. Whole blood samples do not freeze and need to be stored within 48 hours at 2°C to 8°C.

Test Method

Please read the instructions carefully before testing. All reagents must be returned to room temperature prior to testing, which must be conducted 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) to Vail filled with test card, add 2 drops (~ 60L) of sample buffer storage 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 (C line) 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 watch band cannot be seen on the red watch band. The test line (T line) is below the reference line (R line), quality control (C) line and reference line. Lines (R lines) are colored.

Limitation of Test Method

1. This kit is for qualitative analysis only for invitro diagnostic purposes.
2. Please add appropriate test samples. If the sample size is too large or too small, the result may be incorrect.
3. Hemolysis, lipids in the blood, jaundice, sample contamination, etc., may affect the test results, so it must be avoided as far as possible.
4. The test results of the reagent are for clinical reference only, and cannot 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.
2. This product is disposable and can't be reused.
3. Please read carefully before operation and strictly follow the instructions of reagent for experimental operation.
4. Please avoid conducting experiments under harsh environmental conditions (84 disinfectants, sodium hypochlorite, acid, alkali, acetaldehyde, other corrosive gases with high concentration, dust, etc.). Disinfection of the laboratory must be carried out after the experiment.
5. All samples and reagents used shall be considered as potentially infectious substances and shall be discarded in accordance with district 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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