The TOXO IgG/IgM Rapid Test Kit is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii in human whole blood, serum or plasma.
This kit is intended to be used as a screening test and as an aid in the diagnosis of infection with T. gondii. Any reactive specimen with the TOXO IgG/IgM Rapid Test Kit must be confirmed with alternative testing method(s) and clinical findings.
Toxoplasma gondii (T. gondii) is an obligate intracellular protozoan parasite with a worldwide distribution1, 2. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism3.
A variety of serological tests for antibodies to T. gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are: the SabinFeldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluo rescence and ELISA4-7. Recently, lateral flow chromatographic immune Rapid Test such as the Toxo IgG/IgM Cassette Rapid Test has been introduced to the clinic for the instant detection of T. gondii infection.
• The Toxo IgG/IgM Test is intended for use with human whole blood, serum or plasma specimens only.
• Only clear, non-hemolyzed specimens are recommended for use with this test. Serum or plasma should be separated as soon as possible to avoid hemolysis.
• Perform testing immediately after specimen collection. Do not leave specimens at room temperature for prolonged periods. Serum and plasma specimens may be stored at 2-8°C for up to 3 days. For long term storage, specimens should be kept below -20°C.
• Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Avoid repeated freezing and thawing of specimens.
• If specimens are to be shipped, pack them in compliance with all applicable regulations for transportation of etiological agents.
• Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results
Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before use.
About Us
Dewei Medical Equipment Co., Ltd. is a high-tech enterprise specialized in developing and marketing of Medical Consmuables like Clinical Laboratory analyzer and reagents, Hematology Analyzer and Reagents, Washing Solutions, Urine Sediment Reagents and DNA/RNA Preservation Kits.
During the special period, Dewei also develop the reagent kits, like Virus Transport Medium with swab, Rapid test and Saliva Collection Kits.
Dewei products are widely used in hospital clinics, disease control centers, blood banks, veterinary clinics, scientific research center and college laboratories.
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