LSH Ab Test Canine Leishmania Canis Rapid Test Kit is a rapid chromatographic immunoassay method for the qualitative detection of Leishmania IgG and IgM antibodies in human whole blood, serum or plasma. The purpose is to assist in the diagnosis of visceral leishmaniasis.
LSH Ab Test Canine Leishmania Canis Rapid test Kit is a rapid chromatographic immunoassay method for the qualitative detection of Leishmania IgG and IgM antibodies in human whole blood, serum or plasma. The purpose is to assist in the diagnosis of visceral leishmaniasis.
LSH Ab Test Canine Leishmania Canis Rapid Test Kit
Dog's serum, plasma and whole blood specimen
800 test kits
1 week after Get payment
10 test kits/Packing box
2-30°C, DO NOT FREEZE. Do not store the test kit in direct sunlight.
1. One-step whole blood, serum and plasma testing.
2. Simple operation, non-professional on-site inspection.
3. The detection process is fast, and the result will be displayed in about 15 minutes.
4. The test time is less than or equal to 10 seconds, and it can detect 270 samples per hour at the fastest.
5. The detection equipment is compact, easy to carry, mobile terminal operation, cloud platform quality control.
6. The detection sensitivity is high, comparable to that of enzyme-labeled kits.
• Test devices
• Single Buffer
The LSH Ab Test Canine Leishmania Canis Rapid Test Kit is used to detect Leishmania antibodies in whole blood, serum or plasma. After the Leishmania antibody is absorbed by the cellulose pad, it moves and combines with the gold colloidal complex of the Leishmania antigen of the conjugate pad to form an Ag-Ab complex. This complex and Leishmania antigen (Ag) form an Ag-ab-Ag direct sandwich binding on the nitrocellulose membrane. The test result can appear on the control line and the detection line using the principle of immunochromatography.
Strage and stablity
The kit can be stored at room temperature (2-30°C). The test kit is stable through the expiration date (18 months) marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight.
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- Allow all materials, including specimen and test device, recover to 15-25℃ before running the assay.
- Take out the test card from the foil pouch and place it horizontally.
- Collect 20μL of the prepared specimen (serum, plasma or whole blood) into a vial of assay buffer and mix well. Then drop 3 drops (approx. 120μL) of the diluted sample into the sample hole "S" of the test card.
- Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid.
INTERPRETATION OF ASSAY RESULT
- Positive (+): Whether the T line is clear or fuzzy, the "C" line and the region "T" line are present.
- Negative (-): Shows only the sharp C line. No T line.
- Invalid: no color lines in zone C. Whether the T line appears or not.
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