Infectious Disease

Human Immunodeficiency Virus 1/2 (HIV 1/2) Antibody Rapid Test

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Results in 10 minutes Easy to use Multiple sample types: Whole Blood, Serum, or Plasma

Rapid immunochromatographic test for the qualitative detection of antibodies to HIV-1 and HIV-2 in whole blood, serum, or plasma.

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CE
Marked
ISO 13485

Why Test for HIV-1/2 Antibodies?

Early detection of HIV-1 and HIV-2 antibodies is crucial for initiating timely antiretroviral therapy, preventing disease progression, and reducing transmission rates. This rapid test provides a convenient and reliable screening method for HIV infection.

Inside NomoFlow™: The Source of This Test's Superior Performance

The HIV 1/2 Antibody Rapid Test demonstrates high sensitivity and specificity compared to reference ELISA methods.

Performance Characteristics

Analyte Sensitivity (PPA) Specificity (NPA) Overall Agreement
HIV-1/2 Antibodies 99.5% (95% CI: 98.2% - 99.9%) 99.2% (95% CI: 98.5% - 99.6%) 99.3%

Relevant studies and publications will be available here soon.

Time to Result 10 minutes
Sample Type Whole Blood, Serum, Plasma
Kit Size 25 Tests/Kit
Storage Condition 2-30u00b0C
Shelf Life 24 Months
Included Materials Test devices, Buffer, Package insert
Required Materials (Not Included) Specimen collection containers, Timer
Certifications CE, ISO 13485

1

Add Sample

Add the appropriate amount of whole blood, serum, or plasma to the test device.

2

Incubate

Incubate for 10 minutes at room temperature.

3

Read Result

Observe the presence or absence of colored bands to determine the result.

Human Immunodeficiency Virus 1/2 (HIV 1/2) Antibody Rapid Test

  • Catalog Number: VIR-HI2AB

Download product documents for detailed information.

Support

Frequently Asked Questions

Direct answers regarding clinical performance, workflow, and logistics.

This test can be used with whole blood, serum, or plasma samples.
Results are available in just 10 minutes.
A positive result indicates the presence of antibodies to HIV-1 and/or HIV-2, suggesting an HIV infection. Confirmation with a more specific assay is recommended.

Have more specific technical or clinical questions?

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