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Introducing the revolutionary FDA approved rapid point-of-care test, the Alere Determine Antibody Test HIV Detection Whole Blood Rapid Test Kit. This groundbreaking 4th generation test is designed to detect both HIV-1/2 antibodies and free HIV-1 p24 antigen, providing unparalleled accuracy and efficiency in HIV diagnosis.
With its unique capability to identify HIV infection earlier than traditional 2nd and 3rd generation antibody-only tests, the Alere Determine Antibody Test empowers healthcare providers to diagnose HIV with increased precision and timeliness. By detecting both antibodies and the p24 antigen, which is present in high levels during the early stages of infection, this test enables early detection of HIV, ensuring individuals can seek medical care and intervention sooner.
This point-of-care test is designed for ease of use, providing rapid results in a matter of minutes. Its simplicity and convenience make it an invaluable tool in various healthcare settings, including clinics, hospitals, and community-based testing programs. With this test, healthcare providers can quickly and accurately diagnose HIV infection, initiating appropriate treatment plans and support for affected individuals.
The Alere Determine Antibody Test goes beyond conventional tests by offering superior sensitivity and specificity, reducing the risk of false-positive or false-negative results. Its FDA approval signifies its compliance with rigorous quality and performance standards, ensuring reliability and confidence in its diagnostic outcomes.
Not only does this test improve diagnostic accuracy, but it also has a profound impact on public health. By identifying HIV infection earlier, it enables prompt access to medical care, support services, and preventive measures. Early intervention helps to manage the virus effectively, reduce transmission rates, and improve the overall health outcomes of individuals living with HIV.
The Alere Determine Antibody Test HIV Detection Whole Blood Rapid Test Kit represents a significant advancement in HIV diagnosis. Its cutting-edge technology, combined with its FDA approval and ability to detect HIV earlier than previous generation tests, makes it an essential tool in the fight against HIV/AIDS. With this rapid and reliable point-of-care test, healthcare providers can make informed decisions, provide timely care, and contribute to better health outcomes for individuals affected by HIV.
- Introducing the first FDA approved rapid point-of-care test that detects both HIV-1/2 antibodies and free HIV-1 p24 antigen.
- This 4th generation test has the ability to identify HIV sooner than conventional rapid tests which rely solely on the presence of HIV-1/2 antibodies.
- Built-in quality controls to let you know the test is working.
- Can be performed with variety of sample types.
- Test Strips are provided in an aluminum ziplock pouch and can be separated from each other by tearing along the perforated lines.
- Each test strip has a cover that is to be removed for sample application and visualization of test results
- Chase Buffer included for use with whole blood samples.
Product Specifications
| Country of Origin: | USA |
|---|---|
| Application: | Rapid Test Kit |
| CLIA Classification: | CLIA Waived for Fingerstick Whole Blood / CLIA Moderate Complexity for Venous Whole Blood, Serum, Plasma |
| Reading Type: | Visual Read |
| Sample Type: | Whole Blood / Serum / Plasma Sample |
| Test Format: | Test Card Format |
| Test Method: | Lateral Flow Method |
|---|---|
| Test Name: | HIV Detection |
| Test Type: | Antibody Test |
| Time to Results: | 20 Minute Results |
| Disposable: | Yes |