Results in Minutes

Human Immunodeficiency Virus 1/2/O (HIV 1/2/O) Antibody Rapid Test Device (Whole Blood/Serum/Plasma)

Quick detection of HIV-1/2/O antibodies using whole blood, serum, or plasma for timely HIV diagnosis.

CE Certified
ISO 13485
Main image of Human Immunodeficiency Virus 1/2/O (HIV 1/2/O) Antibody Rapid Test Device (Whole Blood/Serum/Plasma)

Why Choose reOpenTest Infectious Disease Kits?

Our tests are engineered for accuracy, reliability, and ease of use, ensuring confidence in every result.

Broad HIV Detection

Detects antibodies to HIV-1, HIV-2, and HIV-O subtypes for comprehensive screening.

Rapid Turnaround Time

Provides results in just 15-20 minutes, facilitating quick clinical decisions.

Easy to Use

Simple procedure suitable for point-of-care testing in various settings.

Product Overview

The Human Immunodeficiency Virus 1/2/O (HIV 1/2/O) Antibody Rapid Test Device is a qualitative immunoassay for the detection of antibodies to HIV-1 and HIV-2 in human whole blood, serum, or plasma specimens. This test is designed for professional use to aid in the diagnosis of HIV infection.

Technical Specifications

Detection Target HIV-1/HIV-2/HIV-O antibodies
Sample Type Whole Blood, Serum, Plasma
Methodology Immunochromatography
Detection Range Positive/Negative
Reaction Time 15-20 minutes
Storage Conditions 2-30u00b0C
Shelf Life 24 months

Procedure & Interpretation

Step-by-Step Procedure

  1. Collect a whole blood, serum, or plasma sample.
  2. Apply the sample to the test device.
  3. Add the provided buffer solution.
  4. Read the results after 15-20 minutes.
  5. Interpret the results based on the appearance of control and test lines.

Result Interpretation

Positive Result
Positive: The presence of control and one or more test lines indicates a positive result for HIV-1/2/O antibodies.
Negative Result
Negative: The presence of only the control line indicates a negative result.
Invalid Result
Invalid: If the control line does not appear, the test is invalid and should be repeated.

Frequently Asked Questions

Early detection allows for prompt initiation of antiretroviral therapy, improving patient outcomes and reducing the risk of transmission.

No, this test is intended for professional use by trained healthcare providers in clinical settings.

Store the test kit at 2-30u00b0C (36-86u00b0F) and protect it from freezing. Do not use the test after the expiration date.

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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