Canine Leishmania Antibody (LSH Ab) Test Kit is a sandwich side-flow immunochromatography used to qualitatively detect Leishmania antibody (LSH Ab) in dog serum.
Canine Leishmania Antibody (LSH Ab) Test Kit is a sandwich side-flow immunochromatography used to qualitatively detect Leishmania antibody (LSH Ab) in dog serum.
The FUSIDA Leishmania Ab rapid test is based on sandwich lateral flow immunochromatography. The test device has a test window. The test window has an invisible T (test) area and C (control) area. When the sample is applied to the sample hole on the device, the liquid will flow laterally across the surface of the test strip. If there are enough Leishmania antibodies in the sample, a visible T-band will appear. The C-band should always appear after applying the sample, indicating a valid result. In this way, the device can accurately indicate the presence of Leishmania antibodies in the sample.
Components | Specification | ||
1T/box | 20T/box | 25T/box | |
Reagent card | 1 | 20 | 25 |
Diluent pipe | 1 | 20 | 25 |
Instruction | 1 | 1 | 1 |
Note: swabs are complimentary separately according to package specifications.
【Storage and expiration date】
The kit is stored at 2-30℃. Do not freeze. Valid for 24 months; After the kit is opened, the reagent should be used as soon as possible.
【Sample requirement】
1. Sample: Dog (cat) serum.
2. Samples should be tested on the same day; Samples that cannot be tested on the same day should be stored at 2-8 ° C, and those that exceed 24 hours should be stored at -20 ° C.
【Inspection method】
- Using a pipette 1 Collect the dog's serum, plasma or whole blood (fresh or stored at 2-8 ° C and used within 3 days) into the centrifuge tube as a sample.
- Remove the cassette from the foil bag and place it horizontally.
- Use a pipette 2 to gradually drop serum, plasma, or whole blood (blow 5μl) into the sample hole.
- Wait for the sample to be fully absorbed into the sample hole. Then add 2 drops of measuring buffer. Wait 5-10 minutes and explain the result. The result was deemed invalid 10 minutes later.
Positive: Both the quality control line (C line) and the test line (T line) appear
Negative: Only the quality control line (C line) is available
Invalid: Quality control line does not appear, take a new device to retest
1. This product is only used for qualitative testing and does not indicate the virus level in the sample.
2. Test results of this product are for reference only and should not be used as the sole basis for diagnosis and treatment, but should be made by a physician after evaluating all clinical and laboratory evidence.
3. A negative result may occur if the viral antigen present in the sample is below the detection limit of the assay, or if the antigen detected at the disease stage at which the sample was collected is not present.
4. The operation should be carried out in strict accordance with the instructions. Do not use expired or damaged products.
5. The test card should be used within 1 hour after opening; If the ambient temperature is higher than 30 ° C or more humid, it should be used immediately.
6. If the T line has just begun to show color, and then the line color gradually fades or even disappears, in this case, the sample should be diluted several times and tested until the T line color is stable.
7. This product is a disposable product. Do not reuse it.