See now human immunodeficiency virus type 1 and 2 (hiv-1/2) antibody test is a rapid and convenient immunochromatographic in vitro assay. It is used for detection of antibodies to hiv-1/2 in human serum, plasma or whole blood.
30 cassettes in a plastic box.
Specification Strength/ Size Packing Size Packed In HIV 1 & 2 Card Test Triline 50 Tests 50 Box Pack
General Information One-Step HIV Ab Rapid Test is to detect the antibodies in serum, plasma or whole blood. Applied highly purified HIV recombinant proteins: gp120 ,gp41 and gp36 antibody, detect HIV type1,type2 with combining or separate test lines at one time. Sensitivity : 100% , Specificity : 100% Specimen : Serum , Plasma ,Whole Blood , or Urine Reading Time : 10 min
Product Description One-Step HIV1/2 Rapid Test One-Step HIV1/2 Rapid Test is to detect the antibodies against HIV 1/2 in serum, plasma or whole blood.General InformationNo instruments neededApplied highly purified HIV recombinant proteins : p24 ,gp41 and gp36Detect HIV type1 and type2 with separate test lines at one timeSensitivity : 99.9% , Specificity : 99.5%Specimen : Serum , Plasma or Whole Blood , or UrineReading Time : 10 min Product Feature format:strip/cassette/uncut sheet MOQ:1000pcs sensitivity:99.9% specificity:99.5% specimen:WB/S/P Product Specification/Models package:neutral pouch bulk package/OEM package Application One-Step HIV1/2 Rapid Test is to detect the antibodies against HIV 1/2 in serum, plasma or whole blood. Payment T/T and western union Delivery 7-15 work days Origin China Minimum Order 1000pcs
Uncut Sheet HIV 1/2 Tri-Lines Rapid Test Package:30sheets/pouch Specimen:Whole blood/Serum/plasma INTENDED USE The HIV-1/2 Rapid Screen Test (RST) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum/plasma and whole blood. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA. PRECAUTION 1.For in vitro diagnostic uses only. 2.All patient samples should be treated as if capable of transmitting diseases. 3.Do not use test kit beyond expiration date. 4.Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results. SUMMARY AND EXPLANATION OF THE TEST It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens. PRINCIPLE HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma and whole blood. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.
The human immunodeficiency virus (HIV) is a retrovirus that infects cells of the immune system, destroying or impairing their function. As the infection progresses, the immune system becomes weaker, and the person becomes more susceptible to infections. The most advanced stage of HIV infection is acquired immunodeficiency syndrome (AIDS). It can take 10-15 years for an HIV-infected person to develop AIDS. The general method of detecting infection with HIV is to observe the presence of antibodies to the virus by an EIA method followed by confirmation with Western Blot. One step hiv 1 rapid test is a simple, visual qualitative test that detects antibodies in human Whole Blood/serum/plasma. The hiv test kit 1&2 test is based on immunochromatography and can give a result within 15 minutes. Principle of hiv 1 ab test The One Step HIV AbTest is a qualitative membrane strip based immunoassay for the detection of HIV antibodies in Whole Blood /Serum / Plasma. In this test procedure, recombinant HIV antigen is immobilized in the test line region of the device. After a Whole Blood /Serum / Plasma specimen is placed in the specimen well, it reacts with HIV antigen coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized HIV antigen. If the specimen contains HIV antibodies, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain HIV antibodies, a colored line will not appear in this region indicating a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.
The ADVIA Centaur HIV 1/O/2 Enhanced assay is an antigen bridging microparticle chemiluminometric immunoassay used for the detection of antibodies to the human immunodeficiency virus type 1, including Group O, and/or type 2 in serum or plasma. The ADVIA Centaur HIV 1/O/2 Enhanced assay uses yeast recombinant derived antigens corresponding to the viral envelope and core proteins. Recombinant antigens include an HIV-1 envelope protein (gp41/120), an HIV-1 core protein (p24), and an HIV-2 envelope protein (gp36). A synthetic peptide is added for the detection of antibodies to HIV-1 group O. The primary purpose of the ADVIA Centaur HIV 1/O/2 Enhanced essay is to aid in the diagnosis of HIV infection and AIDS. Specimens that are initially reactive should be retested in duplicate. Repeat reactivity is highly predictive of the presence of antibodies to HIV-1 and/or HIV-2 in specimens from people at risk for HIV infection and should be followed up with appropriate supplemental tests for rapid hiv kit and HIV-2 antibodies before making a diagnosis of HIV infection. Product Description of hiv abs test This panel consists of six members, manufactured from human serum or plasma, with a range of concentrations of HIV antibodies and p24 antigen. Panel members were filtered through a 0.2 micron filter. ProClin�® (0.1%) was added as a preservative. The human immunodeficiency virus is the causative agent of acquired immunodeficiency syndrome (AIDS). AIDS was first described in the United States in 1981 and has become one of the leading causes of death worldwide. Despite educational efforts directed towards reducing the transmission of AIDS and increased advancements in treatment, the number of AIDS cases continue to increase. By the year 2010, it is estimated that there will be at least 45 million new human immunodeficiency virus (HIV) infections worldwide.
The test shows the presence in blood or serum of HIV antibodies (both type 1 and type 2).
Hiv test kit 99% above sensitivity and specificity Anti-hiv 1/2 or anti-hiv tri-line, which can tell hiv 1 or hiv 2 positive seperately Single pouched, then in bulk or in box