Testsealabs Disease Test Typhoid IgG/IgM Test
Short Description:
The Typhoid IgG/IgM Test Cassette is a rapid chromatographic immunoassay for the qualitative detection of antibody (IgG and IgM) to typhoid in whole blood/serum/plasma to aid in the diagnosis of typhoid bacillus infection.
 Rapid Results: Lab-Accurate in Minutes |
Lab-Grade Precision: Reliable & Trustworthy |
| Test Anywhere: No Lab Visit Required |
Certified Quality: 13485, CE, Mdsap Compliant |
| Simple & Streamlined: Easy-to-Use, Zero Hassle |
Ultimate Convenience: Test Comfortably at Home |
Product Detail:
- High Sensitivity and Specificity
Designed to accurately detect H.Pylori Ag Test(Feces), providing reliable results with minimal risk of false positives or false negatives. - Rapid Results
The test provides results within 15 minutes, facilitating timely decisions regarding patient management and follow-up care. - Easy to Use
The test is simple to administer with no need for specialized training or equipment, making it suitable for use in various healthcare settings. - Portable and Ideal for Field Use
The compact and lightweight design of the test kit makes it ideal for mobile health units, community outreach programs, and public health campaigns.
Test Procedure:
Results Interpretation
Positive
- Control line (C) and at least one test line (T1 or T2) appear on the membrane.
- Appearance of the T1 test line indicates the presence of typhoid-specific IgM antibodies.
- Appearance of the T2 test line indicates the presence of typhoid-specific IgG antibodies.
- If both T1 and T2 lines appear, it indicates the presence of both typhoid-specific IgG and IgM antibodies.
- Note: The intensity of the test line correlates with antibody concentration—the weaker the concentration, the fainter the line.
Negative
- One colored line appears in the control region (C).
- No apparent colored line appears in the test line region (T1 or T2).
Invalid
- Control line (C) fails to appear.
- Possible reasons: Insufficient specimen volume or incorrect procedural techniques.
- Action: 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.
