Audited Supplier
101034
Biological Diagnostics
Ivd Rapid Test Kits
CE, MSDS, ISO13485
Adult
40PCS/Box or 25PCS/Box;
1000PCS
24 Months
4-30°c
Cassette
Available
Serum/Plasma
Infectious Disease Test
Testsealabs
Carton
66*36*56.5cm
China
3822190090
Product Description
Testsealabs Leishmania IgG/IgM Antibody Rapid Test Kit
(serum / plasma)
(serum / plasma)
Intended Use
The One Step Leishmania IgG/IgM Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to the subspecies of the Leishmania donovani (L.donovani), the Visceral leishmaniasis causative protozoans, in Whole Blood /Serum / Plasma.
It is intended to be used as a screening test and as an aid in the diagnosis of the disease of Visceral leishmaniasis.
Test Procedure:
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30ºC (59-86ºF) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2. Place the test device on a clean and level surface.
3. Hold the dropper vertically and transfer 1 drop of specimen(approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer.
4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Notes:
Applying sufficient amount of specimen is essential for a valid test result. If migration (the wetting of membrane) is not observed in the test window after one minute, add one more drop of buffer to the specimen well.
Interpretation of Results
Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of Leishmania specific IgM antibodies. The appearance of T1 test line indicates the presence of Leishmania specific IgG antibodies. And if both T1 and T2 line appear, it indicates that the presence of both Leishmania specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is.
Negative: One colored line appears in the control region(C).No apparent colored line appear in the test line region.
Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
FAQs:
Q: What are your price?
A: Our price are subject to change depending on supply and other market factors. We will send you an updated price list after your company contact us for further information.
Q: Do you have a minimum order quantity?
A : Yes, Our MOQ is 1000pcs.
But for new customers, we have three chances to order trial order, the quantity can be lower than our MOQ, you can feel free to contact us to place a trial order.
Q: Can you supply the relevant documentation?
A: Yes, we can provide most documentation including certificates and other export documents where required.
Q: Can you make OEM or ODM service?
A: Yes. We can accept OEM service. Meanwhile it's also welcome to choose our ODM products.
