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HIV0008 HIV test kit

HIV0008 HIV test kit

HIV0008 HIV test kit

Product catalog summary
Intended Use: The HIV 1+2 test is a rapid chromatographic immunoassay designed for the qualitative detection of antibodies to HIV type 1 and type 2 in whole blood, serum, or plasma. It aids in diagnosing HIV infection.
Materials Provided: The kit includes 25 sealed pouches with test devices, desiccant pouches, extraction tubes, and an extraction buffer in a dropper bottle. A leaflet with instructions is also included. A timer is required but not provided.
Summary: HIV is the causative agent of AIDS, with HIV 1 and HIV 2 being the primary types. The test detects antibodies to these viruses, which is a common method for determining exposure to HIV. The test uses latex conjugate and recombinant HIV proteins to detect antibodies in blood, serum, or plasma.
Principle: The test is a membrane-based immunoassay. The specimen reacts with HIV antigen-coated particles, migrating on the membrane by capillary action. A colored line in the test line region indicates a positive result, while no line indicates a negative result. A control line confirms the test's validity.
Precautions: The kit is for in vitro use only. Do not mix components from different lots, use expired kits, or reuse components. Handle specimens as potentially infectious, wearing gloves and following proper disposal procedures.
Storage and Stability: Store the kit at 2℃ to 30℃, away from sunlight, moisture, and heat. Use patient samples immediately after collection for best results.
Test Procedure: Add 2-3 drops of the sample to the cassette's well. For whole blood, add 1 drop and 2 drops of wash buffer. Read results within 15-20 minutes.
Interpretation of Results: A single line in the control region indicates a negative result. A line in both the control and test regions indicates a positive result. No control line means the test is invalid.
Quality Control: A procedural control is included. Positive and negative controls are recommended for verifying test performance.
Limitations: The test is qualitative and should not be the sole criterion for HIV diagnosis. Negative results do not rule out HIV infection, and further testing is recommended if symptoms persist.
References: The document cites several studies and articles related to HIV research and testing strategies.
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Catalog excerpts

HIV0008 HIV test kit-1

Neo-nostics (Suzhou) bioengineering Co. ,Ltd

 Open the catalog to page 1
HIV0008 HIV test kit-2

Test Item NO. CategoryType Specimen 050203701 Infectious diseases Dengue IgG&IgM Dengue NS1 Zika IgG&IgM Zika NS1 Scrub Typhus IgG/IgM Schistosome-AB SFTSV TOX IgG/IgM HAV IgM-AB Malaria pf/pv HCV-AB TP-AB HBSAG Ebola cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip cassette/strip w/s/p w/s/p w/s/p w/s/p Serum w/s/p Serum w/s/p w/s/p w w/s/p w/s/p w/s/p Nasal Wipe The body is the capital of the revolutionNeo-nostics (Suzhou) bioengineering Co. ,Ltd...

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HIV0008 HIV test kit-3

HIV 1+2 Rapid Test Kit (Serum / Plasma/ Whole Blood) INTENDED USE The HIV 1+2 test a rapid chromatographic immunoassay for the qualitative detection of antibodies to Human Immunodeficiency Virus (HIV) type 1 and type 2 in whole blood, serum or plasma to aid in the diagnosis of HIV infection. 25 Individual sealed pouches, each containing: ■ Test device ■ Desiccant pouch ■ Extraction tubes One extraction buffer in a dropper bottle (6mL): 0.01M phosphate buffer saline (PBS). Leaflet with instructions for use. For in vitro diagnostic use only. For professional use only. SUMMARY HIV is the etiologic...

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HIV0008 HIV test kit-4

Neo Nostics (Suzhou) Bioengineering Co.Ltd. A procedural control is included in the test. A colored line appearing in the control line region (C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique. Control standards are not supplied with this test Cassette; however, it is recommended that positive and negative controls be tested as a good laboratory practice to confirm the test procedure and to verify proper test performance. 1. The HIV 1+2 test kit (Whole Blood/Serum/Plasma) is for in vitro diagnostic...

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