2019 Coronavirus Disease Neutralizing Antibody Rapid Test Kit Card Efficient

Storage temperature is 2℃ ~ 30℃, effective for 12 months.
Aluminum foil bags are valid for 1 hour.
Production Lot Number: Refer to the label for details.
Expiry date: Refer to the label for details.

Sample Requirements

1. Collection of serum, plasma or whole blood samples.
2. Sediment or plankton in the sample may 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 a medical expert is required. Serum/serum/plasma tests are recommended. Whole blood samples from patients can also be used for rapid testing in emergency or special situations.
5. Serum and plasma samples should not be kept at room temperature for more than 8 hours.
Can be stored for 5 days from 2 °C to 8°C, less than -20°C can be stored for 6 months, but please avoid repeated freezing melting. Blood samples are ice-free and must be kept at 2°C ~ 8°. C within 48 hours.

Test Method

Please read the instructions carefully before the test. All reagents should be returned to room temperature prior to test, which must be carried out at room temperature.
1. Remove the test card from the package and use it within 1 hour.
2. Add 20L sample (serum, plasma or whole blood) to the filling hole of the test card, add 2 drops (~ 60L) of sample buffer memory and start timing.
3. Reaction at room temperature for 10 to 15 minutes, read the results. Invalid after 20 minutes.

Interpretation of Test Results

Test card explanation:
1. Invalid result: The response line of quality management line (Line C) is not invalid and needs to be tested again.
2. Negative result: the test line (T line), color appearance is greater than the reference line (R line), quality management line (C line) and reference line (R line) color.
3. Positive results: There is no red band on the test line (T line), the red band on the test line (T line) is lower than the reference line (R line), and the quality management line (C line) and the reference line (R line) are colors.

Limitation of Test Method

This kit is for qualitative testing and Invitro assisted diagnosis only.
2. Confirm that the appropriate number of test samples has been added. If the sample size is too large or too small, the result may be incorrect.
3. Hemolysis, lipids, jaundice, and contaminated samples may affect the results and must be avoided.
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. A final diagnosis of the disease must be made after a comprehensive evaluation of 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. Do not perform the experiment under harsh environmental conditions (84 disinfectant, sodium hypochlorite, acid, alkali, acetaldehyde, other highly corrosive gases, dust, etc.). Please disinfect in laboratory after experiment.
5. All samples and reagents used are treated as potentially infectious substances and are disposed of in accordance with regional regulations.
6. The reagent must be used within the expiry date stated on the package. To prevent moisture, the test card must be used as soon as possible after it is removed from the foil bag.

Logo interpretation

Basic Information

ZHONGXIU SCIENCE AND TECHNOLOGY CO.,LTD

Dingluan industrial zone ,Changyuan City,453400,P.R.CHINA

Tel:+86-371-55016575

Email:zosbio@zosbio.com

Web:www.zosbio.com

SUNGO Europe B.V.

Olympisch Stadion 24, 1076DE Amsterdam, Netherlands

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