
Dual-line detection for HIV-1 and HIV-2 antibodies
Results in 15 minutes quick and efficient testing
Works with whole blood, serum, or plasma samples
Easy-to-use with dropper and buffer provided
Room temperature storage (2C to 30C)
Evaluated by National Institute of Biologicals (India)
High correlation with ELISA & other rapid tests
The test detects antibodies targetinggp41 and gp120 antigens(for HIV-1) andgp36 antigen(for HIV-2). When the sample reacts with these coated antigens, distinct red-magenta lines appear in their respective areas if antibodies are present. An internal control line ensures test validity.
Individually pouched test devices
Assay buffer vials
Disposable droppers
Silica gel for moisture control
Alcohol swabs and sterile lancets (in select packs)
Product insert (IFU)
Available Pack Sizes:25Tests & 50Tests
(Custom packaging with lancets and swabs also available)
This test is intended for professional in vitro diagnostic use. It is ideal for use in clinical laboratories, hospitals, blood donation camps, and diagnostic centers.
The test works with whole blood, serum, or plasma. It supports both venipuncture and finger-prick blood collection.
The test has demonstrated100% sensitivity and 100% specificity during internal and external evaluations, including by the National Institute of Biologicals (NIB).
Two Lines (C + HIV-1 or C + HIV-2): Positive
Three Lines (C + HIV-1 + HIV-2): Positive for both
One Line (C only): Negative
No Control Line (C): Invalid, repeat with new test
A positive result is preliminary and should be confirmed with a Western Blot or other confirmatory test sin accordance with national HIV testing guidelines.
Store the kits in a sealed pouch between2C and 30C. Do not freeze. Use the test before the expiration date indicated.
No. The test issingle-use onlyand should be safely discarded after use as per biomedical waste protocols.
The test has been validated by leading national bodies such as the NIB (India)and is manufactured in an ISO-certified facility. Please refer to local regulatory approval requirements for use in your region.
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