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| Product Name | Hantavirus IgG/IgM Antibody Rapid Test Kit |
| Catalog No. | DBX-QCY-1682 |
| Description | This kit is used for qualitative detection of Hantavirus IgG antibody and IgM antibody in human serum, plasma and whole blood samples in vitro, which plays an important role in the early diagnosis and treatment of Hantavirus infection, and can assist in the diagnosis of Hantavirus infection in clinical practice. |
| Kit Components | Test card Sample diluent buffer sterile lancets Dropper Alcohol pad Instructions for use |
| Sample Type | Serum, plasma, cell culture supernatant |
| Sample Preparation | Whole blood samples collection: Fingertip or venous blood was collected using anticoagulant tubes or blood collection tubes pre-added with anticoagulant (heparin, EDTA, sodium citrate and other anticoagulants are recommended), and then shaken for later use. The sample should be used as soon as possible after collection: If it cannot be tested immediately, the sample can be refrigerated at 2-8 °C, and the whole blood sample should be tested within 3 days. Serum/plasma sample collection: Venous blood is collected, after blood coagulation, the supernatant is drawn directly or after centrifugation, which is the serum. Blood is collected with a collection tube or anticoagulant tube added with anticoagulant (it is recommended to use heparin, EDTA, sodium citrate, etc.), and the upper layer of light yellow clear liquid is taken after centrifugation or resting, which is the plasma sample. If the serum/plasma samples cannot be tested in time, they should be refrigerated at 2-8° C for two weeks. If long-term storage is required, they should be refrigerated at -20 °C and returned to room temperature before testing. Note: A high concentration of jaundice samples (the visual appearance of the sample solution is yellow), a high hemolysis sample (free hemoglobin concentration >9g/L), or a visually visible chylous sample will interfere with the interpretation of the test results, so attention should be paid to the appearance of the sample before using the sample. |
| Test Procedure | Take the test card out of the packaging bag and use it within one hour. Place the test card on a clean, level table, and mark it. Test the collected whole blood, serum and plasma: Use a dropper to draw the sample and add 1 drop （10μL）into the sample well (S) of the test card. Then, drop 2 drops sample diluent buffer into the diluent well (D). Start timing. Note: If the liquid doesn’t move to the position of the control area (C) in 2 minutes, add one more drop of the sample diluent buffer into the diluent well. Test for fingertip blood: First, wipe the fingertip with the alcohol pad. Then, place a sterile lancets against the fingertip and press it down slightly with force. Squeeze out a drop of fingertip blood and draw it with a dropper. Add 1 drop （10μL）into the sample well (S) of the test card. Next, drop 2 drops sample diluent buffer into the diluent well (D). Start timing. The final result should be read in 10 minutes. The result read after 20 minutes has no clinical significance. |
| Interpretation of Results | Positive: Two red lines, that is, one red reaction line in the detection area (IgG or IgM) and one in the quality control area (C). Negative: One red line, that is, a red response line appears only in the quality control area (C). Invalid: No red reaction line appears in the quality control area (C). The test is invalid, it is recommended to re-test with a new test card at this time, especially pay attention to whether the added sample is enough. |
| Storage and Transportation | Store the test kit between 2°C~30°C in a place out of direct sunlight, product expiration date 24 months. After the foil pouch is opened, the test card should be used as soon as possible within 1 hour. |
| Precautions | This kit is a disposable in vitro diagnostic reagent, please do not reuse, and do not use expired products. The aluminum foil pouch contains a desiccant and should not be taken internally. Fresh samples are recommended. Components in different lot kits should not be cross-used to avoid erroneous results. The temperature of the experimental environment should be avoided from being too high, and the test card should be restored to room temperature before opening it to avoid moisture absorption. After the test, the used test card, sample diluent, straw, etc. will be disposed of as biomedical waste. Please pay attention to safety measures during operation, such as wearing protective clothing and gloves. As with all diagnostic reagents, the final diagnosis should be made by the physician after taking into account the various test indicators and clinical symptoms. |
For in vitro diagnostic use.
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