Rapid Antibody Test
Leishmania IgG/IgM Antibody Rapid Test
Rapidly detect Leishmania IgG/IgM antibodies in whole blood, serum or plasma.
CE Certified
ISO 13485

Why Choose reOpenTest Infectious Disease Kits?
Our tests are engineered for accuracy, reliability, and ease of use, ensuring confidence in every result.
Detect IgG/IgM
Simultaneous detection of IgG and IgM antibodies.
Multiple Sample Types
Suitable for whole blood, serum, or plasma.
Point-of-Care
Rapid and efficient for point-of-care environments.
Product Overview
The Leishmania IgG/IgM Antibody Rapid Test is a qualitative immunochromatographic assay for the simultaneous detection of IgG and IgM antibodies to Leishmania in human samples. Early detection is crucial for treatment.
Technical Specifications
Detection Target | Leishmania IgG/IgM antibodies |
---|---|
Sample Type | Whole blood, Serum, Plasma |
Methodology | Immunochromatography |
Detection Range | Qualitative (Positive/Negative) |
Reaction Time | 15-20 minutes |
Storage Conditions | 2-30u00b0C |
Shelf Life | 24 months |
Procedure & Interpretation
Step-by-Step Procedure
- Add the sample (whole blood, serum, or plasma) to the test device.
- Add the buffer solution.
- Wait 15-20 minutes.
- Read and interpret the results.
Result Interpretation

Positive:
Presence of both control line and test lines for IgG and/or IgM indicates a positive result.

Negative:
Presence of only the control line indicates a negative result.

Invalid:
If the control line does not appear, the test is invalid.
Frequently Asked Questions
The test detects antibodies to Leishmania, regardless of the clinical form of the disease. Further tests are needed to differentiate between forms.
PCR-based methods may offer higher sensitivity, especially in early stages of infection. This rapid test provides a convenient screening option.
IgM antibodies typically indicate a recent infection, while IgG antibodies suggest past or ongoing exposure. Both are important indicators.
Technical Documents
Download product inserts and brochures for detailed information.
No technical documents are available at this time. Please check back soon.
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