meril quadro hiv 1-2 ab rapid test kit
67 Per piece
Product Overview QUADRO HIV 1-2 Ab is a rapid flow-through in-vitro qualitative assay for the detection of antibodies to HIV-1 and HIV-2 human serum & plasma. QUADRO HIV 1-2 Ab is designed to detect antibodies specific to envelope glycoproteins of HIV-1 and HIV-2 by using unique combination of synthetic and recombinant antigens in the same device differentially. Flow-through-based differential detection of HIV -1 and HIV -2 Synthetic peptides coated on HIV 1 and HIV 2 region Uniquely formulated recobinant proteins coated in HIV 1+2 region
J. Mitra HIV Tri-Dot Kit
17,653 Per Piece
5 Piece (MOQ)
I. HIST Orical review and aetiology of aids (acquired immuno deficiency syndrome)First confirmed case of Aids was identified in 1983 and by 1984 the etiologic agent, the Human Immunodeficiency Virus (HIV), subsequently named HIV-1 was isolated. Shortly afterwards in 1985 another retrovirus subsequently named HIV-2 was isolated in Africa. These two viruses belong to the retrovirus group and are slow viruses. The structure, gene organisation and serological behaviour of HIV-1 & HIV-2 and their complete nucleotide sequence has been determined. This knowledge has laid a foundation for the development of a new assay based on Recombinant DNA technology leading to the differential detection of antibodies to HIV-1 & HIV-2 (if present) in Human Serum or Plasma. Research has shown that antibodies produced against envelope gene are found in infected people as shown in graph, (Fig.-1).HIV TRI-DOT has been developed and designed using gp41, C terminal of gp120 & gp36 representing the immunodominant regions of HIV-1 & HIV-2 envelope gene structure respectively. The device (an immunofiltration membrane) includes a "Built-in Quality Control DOT" which will develop colour during the test, thereby, confirming proper functioning of the device, reagents and correct procedural application. This Control dot is the "Built-in Quality Control." (Fig.2) HIV TRI-DOT has been specially researched, developed and engineered using several thousands of serum/plasma specimens. It has also been evaluated by UNAIDS (WHO) Geneva, using samples of European, Asian, Latin American & African origin. The Sensitivity and Specificity has been extremely high in these samples of diverse origin. The panel used for evaluation of HIV TRI-DOT by Institute of Tropical Medicine, WHO Collaborating Centre in AIDS, Belgium also included HIV-O Virus, which was found reactive with HIV TRI-DOT.2. Intended use The HIV TRI-DOT Test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgM, IgG & IgA) in Human Serum or Plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for anti-HIV-1 & antiHIV-2 and is for in vitro diagnostic use only.3. Description of symbols usedThe following are graphical symbols used in or found on J. Mitra diagnostic products and packing. These symbols are the most common ones appearing on medical devices and their packing. They are explained in more detail in the British and European Standard EN ISO 15223-1:2016.4. Principle of the testHIV antigens are immobilized on a porous immunofiltration membrane. Sample and reagents pass through the membrane and are absorbed into the underlying absorbent. As the patient''s sample passes through the membrane, HIV antibodies, if present, bind to the immobilized antigens. Conjugate binds to the Fc portion of the HIV antibodies to give distinct pinkish purple DOT(s) against a white background. (Fig.-3)
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HIV 1/2 Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Human Immunodeficiency Virus(HIV-1, HIV-2) type 1,type 2 in whole blood, serum or plasma to aid in the diagnosis of HIV infection. Packaging included: 1 Aspen HIV Test Kit, 1 diluent, 1 twist lancet, 1 alcohol swab, 1 pipette Directions For Use: Add 1 drop (25 µl) of Whole Blood to specimen well of test device using dropper/pipette. Then add 2 drop of buffer (40 µl ) Read results in 10 minutes (Do not interpret the result after 20 minutes) Featurs: Results in 10 mins Clinical Sensitivity: 100% Specificity: 99.8% Cert: ISO 13485.
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