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HIV(1+2) Ag/Ab Combo Test Kit (3 Lines)
Cat. No.: RH0210I
【The 4th Generation of ONE STEP HIV antigen and antibodies to HIV-1/2 Test】
The HIV (1+2) Ag/Ab combo rapid test kit is a rapid, qualitative test for the detection of HIV p24 antigen and antibodies to all isotypes (IgG, IgM and IgA) specific to HIV-1 including subtype-O and/or HIV-2 simultaneously in human serum, plasma. The antigens are prepared with proteins to have HIV-1, gp41, gp120 and gp36. For HIV 2, p24 ab & gp36. The HIV (1+2) Ag/Ab Combo Test kit (3lines) is intended for professional use, only for an initial screening test and reactive samples should be confirmed by a supplemental assay such as ELISA or Western Blot test.
HIV (Human Immunodeficiency Virus) is recognized as the etiologic agent of Acquired immune Deficiency Syndrome (AIDS). The virus is transmitted by sexual contact, exposure to infected blood, certain body fluids or tissues, and from mother to fetus or child during the perinatal period. HIV-1 has been isolated from patients with high potential risk of developing AIDS.
HIV-1 appears to be the most common one while HIV-2 is mostly found in patient samples from West African region. Its course is marked by increasing levels of viral replication and the emergence of more virulent viral strains. This process causes the destruction of the immune system. HIV infection is staged by CD4 cell counts and clinical symptoms. Not all people progress through all “stages” and the time frames may also very greatly from person to person.
The 4th generation HIV(1+2) Ag/Ab Combo Test kit (3lines) contains a membrane strip, which is pre-coated with mouse monoclonal Anti-HIV p24 antibody on test line “2” region with gp36 and test line “1” region with recombinant HIV-1/HIV-2 antigens respectively. The mixture of mouse monoclonal anti-HIV p24 antibody and recombinant HIV-1/HIV-2 antigen-colloid gold conjugate form a visible lines (1&2) as the antigen-antibody-antigen or antibody-antigen-antibody gold particle complex with high degree of sensitivity and specificity.
The test lines and control line in the result window have been clearly labeled. For line “2” is for HIV p24 antigen and/or antibodies to HIV-2 and line “2” is for antibodies to HIV-1/HIV-2, and “C” for Control line. All the test lines and control line in the result window are not visible before applying any sample. The control line is used for procedural control and should always appear if the test procedure is performed correctly.
1. Forty pouched cassettes with desiccant and dropper.
2. Blood diluent in a dropper bottle, stored at 2-8°C.
3. One piece of operating instruction.
Add 2 drop (1 drop = 35µl) of sample (serum/plasma) into the sample well. Observe the result in 5-15 minutes.
An internal procedural control is included in the test. Red line will appears in the control region (C).
Negative: No apparent band in the test region (1 and 2), Only one red band appears in the control region (C). This indicates that no HIV p24 antigen and/or antibodies to HIV-1/HIV-2 have been detected.
1) The presence of two lines as control line “C” and test line “2” within the result window indicates a positive result for HIV p24 antigen . The presence of HIV antigen suggests that the infection is at an early stage.
2) The presence of two lines as control line “C” and test line “1” within the result window indicates a positive result for antibodies to HIV-1/HIV-2.
3) The presence of three lines as control line “C”, test line “2” and test line “1” within the result window indicates a positive result for HIV p24 antigen and/or antibodies to HIV-1/HIV-2. The presence of HIV antigen suggests that the infection is at an early stage.
Invalid: If no band appears in the control region(C), regardless of the presence or absence of line in the test region (T1 & T2). It indicates a possible error in performing the test. The test should be repeated using a new device.
Note: Except the red line, no other color line means a positive result. Do not read the results after 30 minutes. Dispose off the used cassette as infectious material.
The detection limit of the HIV(1+2) Ag/Ab Combo Test kit (3lines) is 2IU/ml, which is evaluated by testing the HIV-1 p24 antigen panel from the National institute for Biological Standard and Control.
Store the 4th generation HIV(1+2) Ag/Ab Combo Test Kit (3lines) at temperature ranges 2-30°C in the sealed pouch for the duration of the shelf life period (24months). Refer to the expiration date for stability. Do not freeze.
1. The test is to be used for the qualitative detection of antibodies to HIV.
1. Centers for Disease control: Provisional Public Health Service inter-agency recommendations for screening donated blood and plasma for antibody to the virus causing acquired immunodeficiency syndrome. Morbidity and Mortality Weekly Rep 34: 5-7, 1985.
2. Coffin J, Haase A, Levy JA, et al: What to call the AIDS virus? Nature 321: 10, 1986
3. Popovic, M., et al: Detection isolation and continuous production of Cytopathic Retroviruses (HTLV.Ⅲ) from patients with AIDS and pre-AIDS. Science 1984; 224:497
4. Carison, J. R. et al: AIDS serology testing in low and high risk groups.JAMA1985; 253:3405
5. Centers for Disease contro,Update on Acquired Immune Deficiency Syndrome(AIDS)MMWR 1982; 31:507
6. Gallo, RC, et al: Frequent detection and isolation of Cytopathic Retroviruses (HTLV.Ⅲ) from patients with AIDS and a risk for AIDS.Science.1984; 224:500
Span Biotech Ltd. is a research based company for rapid tests, with strong support from National Key Laboratory of Technology Projects of 10th and 11th Five-Year Plan and Faculty of Life Sciences of HuBei University. SpanBio also housed a R&D team that is developing gene recombination, cell cultivation and protein purification techniques. SpanBio pays strict attention on rapid tests for human being, animal diseases and food safety detection. It provides a number of customized services to professional distributors and partnering affiliates with excellent quality, competitive prices and super service.
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