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700000, Maxim HIV-1Urine EIA kit, 480 Tests
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The FDA Approved Maxim HIV-1 Urine EIA test is an enzyme immunoassay for the in vitro detection of antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) in urine. The test is intended for use in professional laboratory settings as an aid in clinical diagnosis of HIV infection. Before a determination of HIV-1 status can be made, specimens that are repeatedly reactive using this test should be further tested only using the additional, more specific FDA approved Cambridge Biotech Western Blot Kit (PN 98078).
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