Audited Supplier
HITP
IVD Reagent
Rapid Test
Whole Blood/Serum/Plasma
Within 15 Mins
2~30 º C
Immunochromatography
24 Months
Professional Used
Dewei
40tests/Box
1000tests/carton
China
Product Description
INTENDED USE
The HIV 1/2 & Syphilis(TP) Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of antibodies to HIV-1/HIV-2 and antibodies to Treponema Pallidum (TP) in human whole Blood, serum or plasma specimens. This kit is intended for use as an aid in the diagnosis of HIV infection.
PRINCIPLE
The HIV 1/2 Rapid Test detects antibodies to HIV-1/HIV-2 and Treponema Pallidum (TP) through visual interpretation of color development on the internal strip.
Recombinant HIV antigens are immobilized on the test region of the membrane. During testing, the specimen reacts with HIV antigen conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there are sufficient HIV-1/HIV-2 antibodies in the specimen, a colored band will form at the HIV test region of the membrane. The presence of this colored band indicates a positive HIV result, while its absence indicates a negative result.
Specific recombinant TP antigens are immobilized on the test region of the membrane. During testing, the specimen reacts with recombinant TP-specific antigen conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there are sufficient antibodies to Treponema Pallidum (TP) in the specimen, a colored band will form at the SYP test region of the membrane. The presence of this colored band indicates a positive SYP result, while its absence indicates a negative result.
The appearance of a colored band at the C control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
WARNINGS AND PRECAUTIONS
Immunoassay for in vitro diagnostic use only.
Do not use after expiration date.
The test should remain in the sealed pouch until use.
The used test should be discarded according to local regulations.
STORAGE AND STABILITY
The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
The test must remain in the sealed pouch until use.
Keep away from direct sunlight, moisture and heat.
Do not freeze.
Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers or reagents can lead to false results.
OPERATION
Bring tests, specimens, and/or controls to room temperature (15-30°C) before use.
1.Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. For best results, the assay should be performed within one hour.
2.Using the provided disposable dropper, transfer 2 drops of serum/plasma to specimen well (S) of the cassette, then start the timer.
OR
Transfer 1 drop of whole blood specimen to specimen well (S) of the cassette with the provided disposable dropper, then add 1 drop of buffer and start the timer.
OR
Allow 2 hanging drops of fingerstick whole blood specimen to fall into the center of specimen well (S) on the cassette, then add 1 drop of buffer and start the timer.
Avoid trapping air bubbles in the specimen well (S), and do not add any solution to the result area.
As the test begins to work, color will migrate across the membrane.
3. Wait for the colored band(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.
| Storage | 2~30 º C |
| Specimen | Whole Blood/Serum/Plasma |
| Component | Rapid Test + Buffer + Pipettes |
| Principle | Colloidal gold rapid tests |
| Reading | Within 15mins |
| Package | 40tests/box; 1test/box |
| Trademark | Dewei |
| Origin | China |
PRINCIPLE
The HIV 1/2 Rapid Test detects antibodies to HIV-1/HIV-2 and Treponema Pallidum (TP) through visual interpretation of color development on the internal strip.
Recombinant HIV antigens are immobilized on the test region of the membrane. During testing, the specimen reacts with HIV antigen conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there are sufficient HIV-1/HIV-2 antibodies in the specimen, a colored band will form at the HIV test region of the membrane. The presence of this colored band indicates a positive HIV result, while its absence indicates a negative result.
Specific recombinant TP antigens are immobilized on the test region of the membrane. During testing, the specimen reacts with recombinant TP-specific antigen conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there are sufficient antibodies to Treponema Pallidum (TP) in the specimen, a colored band will form at the SYP test region of the membrane. The presence of this colored band indicates a positive SYP result, while its absence indicates a negative result.
The appearance of a colored band at the C control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.
WARNINGS AND PRECAUTIONS
Immunoassay for in vitro diagnostic use only.
Do not use after expiration date.
The test should remain in the sealed pouch until use.
The used test should be discarded according to local regulations.
STORAGE AND STABILITY
The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
The test must remain in the sealed pouch until use.
Keep away from direct sunlight, moisture and heat.
Do not freeze.
Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers or reagents can lead to false results.
OPERATION
Bring tests, specimens, and/or controls to room temperature (15-30°C) before use.
1.Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. For best results, the assay should be performed within one hour.
2.Using the provided disposable dropper, transfer 2 drops of serum/plasma to specimen well (S) of the cassette, then start the timer.
OR
Transfer 1 drop of whole blood specimen to specimen well (S) of the cassette with the provided disposable dropper, then add 1 drop of buffer and start the timer.
OR
Allow 2 hanging drops of fingerstick whole blood specimen to fall into the center of specimen well (S) on the cassette, then add 1 drop of buffer and start the timer.
Avoid trapping air bubbles in the specimen well (S), and do not add any solution to the result area.
As the test begins to work, color will migrate across the membrane.
3. Wait for the colored band(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.
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