Testsealabs HIV 1+2 Antibody Test (Whole Blood/Serum/Plasma)
Short Description:
The Flu A/B+COVID-19 +HMPV Antigen Combo Rapid Test is a rapid chromatographic immunoassay for the simultaneous qualitative detection of antigens specific to Influenza A, Influenza B, SARS-CoV-2 (COVID-19), and Human Metapneumovirus (HMPV) in human nasal/nasopharyngeal specimens. This test aids in the differential diagnosis of acute respiratory infections caused by these pathogens.
 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 HIV 1+2 Antibody Test (Whole Blood/Serum/Plasma), providing reliable results with minimal risk of false positives or false negatives. - Rapid Results
The test provides results within 15–20 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. - Versatile Sample Types
The test works with whole blood, serum, or plasma, providing flexibility in sample collection. - 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:
Positive: Two lines appear. One line should always appear in the control line region (C), and another apparent colored line should appear in the test line region.
Negative: One colored line appears in the control region (C). No apparent colored line appears 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.
