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Convenient AllTest HIV 1.2.O Rapid Test Cassette

Basic Information
Place of Origin: China
Brand Name: Alltest
Certification: CE
Model Number: IHI-T401/IHI-T402/IHI-T402S
Minimum Order Quantity: N/A
Supply Ability: Two weeks
Color: Blue Formot: Cassette
Specimen: WB/S/P Kit Size: Cassette: 40T/Kit, Dipstick: 50T/Kit
Cut-off: See Insert Temperature: 2℃-30℃
High Light:

rapid diagnostic test kits

,

one step rapid test

A rapid test for the diagnosis of Human Immunodeficiency Virus to detect antibodies to HIV type 1, type 2 and Subtype O qualitatively in whole blood.Serum or plasma. For professional in vitro diagnostic use only.

 

Applications:

The HIV 1.2.O Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Human Immunodeficiency Virus (HIV) type 1, type 2 and subtype O in whole blood, serum or plasma to aid in the diagnosis of HIV infection

Description:

 

HIV (Human Immunodeficiency Virus) is the etiologic agent of Acquired Immune Deficiency Syndrome (AIDS). The virion is surrounded by a lipid envelope that is derived from the host cell membrane. Several viral glycoproteins are on the envelope. Each virus contains two copies of positive-sense genomic RNAs. HIV-1 has been isolated from patients with AIDS and AIDS-related complex, and from healthy people with high potential risk for developing AIDS.1 HIV-1 consists of Subtype M and Subtype O. Highly divergent strains of HIV-1 were first recognized in 1990 and grouped provisionally as Subtype O as this variation has similar glycoprotein markers to HIV-1 but a slight variation to the protein marker.
Although rarely compared to HIV-1 and HIV-2, infections caused by Subtype O have so far been identified in Africa (Cameroon), France and Germany. HIV-2 has been isolated from West African AIDS patients and from seropositive asymptomatic individuals.2 HIV-1, HIV-2, and Subtype O all elicit immune responses.3 Detection of HIV antibodies in serum, plasma or whole blood is the most efficient and common way to determine whether an individual has been exposed to HIV and to screen blood and blood products for HIV.4 Despite the differences in their biological characters, serological activities and genome sequences, HIV-1, HIV-2, and Subtype O show strong antigenic cross-reactivity.5,6 Most HIV-2 positive sera can be identified by using HIV-1 based serological tests.
 

How to use:

 

For IHI-T401

Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test dipstick from the sealed pouch and use it as soon as possible.
2. Place the test card on a clean and level desk, then peel off the strip label of the test card, stick the test dipstick onto it as soon as possible before testing.
For Serum or Plasma specimen: Hold the dropper vertically and transfer 1 drop of serum or plasma (approximately 25 ul) to the specimen area, then add 1 drop of buffer(approximately 40 ul), and start the timer, see illustration below.
For Venipuncture Whole Blood specimen: Hold the dropper vertically and transfer 2 drops of whole blood (approximately 50 ul) to the specimen area, then add 2 drops of buffer (approximately 80ul), and start the timer. See illustration below.
For Fingerstick Whole Blood specimen:
 To use a capillary tube: Fill the capillary tube and transfer approximately 50 ul of fingerstick whole blood specimen to the specimen area of test dipstick, then add 2 drops of buffer (approximately 80 ul) and start the timer. See illustration below.
3. Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret the result after 20 minutes.
Note: It is suggested not to use the buffer, beyond 6 months after opening the vial

Convenient AllTest HIV 1.2.O Rapid Test Cassette 0

 

For IHI-T402

 

Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to
testing.
1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it as soon as possible.
2. Place the cassette on a clean and level surface.
For Serum or Plasma specimen: Hold the dropper vertically and transfer 1 drop of serum or plasma (approximately 25 ul) to the specimen area, then add 1 drop of buffer (approximately
40 ul),and start the timer, see illustration below.
For Venipuncture Whole Blood specimen: Hold the dropper vertically and transfer 2 drops of whole blood (approximately 50 ul) to the specimen area, then add 2 drops of buffer (approximately 80ul), and start the timer. See illustration below.
For Fingerstick Whole Blood specimen:
To use a capillary tube: Fill the capillary tube and transfer approximately 50 ul of fingerstick whole blood specimen to the specimen area of test cassette, then add 2 drops of buffer (approximately 80 ul) and start the timer. See illustration below.
To use hanging drops: Allow 2 hanging drops of fingerstick whole blood specimen (approximately 50 ul) to fall into the specimen area of test cassette, then add 2 drops of buffer (approximately 80 ul) and start the timer. See illustration below.
3. Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret the result after 20 minutes.

Convenient AllTest HIV 1.2.O Rapid Test Cassette 1

INTERPRETATION OF RESULTS
(Please refer to the illustration above)
POSITIVE:* Two or three distinct colored lines appear. One line should always appear in the control line region (C), and another one or two apparent colored line(s) should appear in the test line region(s) (T1 and/or T2).
*NOTE: The intensity of the color in the test line region (T1 and T2) will vary depending on the concentration of HIV antibodies present in the specimen. Therefore, any shade of color in the test line region (T1 and/or T2) should be considered positive.
NEGATIVE: One colored line appears in the control region (C). No apparent colored lines appear in the test line regions (T1 and T2).
INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

 

 

Cat. No. Product Description Specimen Format Kit Size Cut-Off Status
IHI-T401 HIV1.2.ORapid Test Cassette WB/S/P Cassette 50T See Insert NON-CE
IHI-T402 HIV1.2.ORapid Test Dipstick WB/S/P Cassette 40T See Insert NON-CE
IHI-T402S HIV1.2.ORapid Test Cassette WB Cassette 1T See Insert

NON-CE

 

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