HIV 1/2 AND P24 Combo Rapid Tets | HIV 317

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SKU:
ATLK-HIV 317
Availability:
Available in Bulk Order of 100 KITS & More
Bulk Quantity:
20T
Format:
Multi-devices
Specimen:
W/S/P
Select Currency //2,225.00

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Description

HIV 1/2 AND P24 Combo Rapid Tets | HIV 317 from Gentaur Diagnostics is available for delivery.NTENDED USE: This HIV (1+2) Ag&Ab ELISA is an enzyme-linked immunosorbent assay (ELISA) for qualitative determination of antigens or antibodies to Human Immunodeficiency Virus (HIV) type 1 and/or type 2 in human serum or plasma. The method is also known as 4th generation ELISA for HIV detection. The kit is intended for screening of blood donors and as an aid for the diagnosis of clinical conditions related to infection with HIV-1 and/or HIV-2. e.g. the acquired immunodeficiency syndrome (AIDS

SUMMARY AND EXPLANATION:

The human immunodeficiency viruses type 1 and type 2 are the etiological agents of the acquired immunodeficiency syndrome (AIDS) and related conditions. HIV has been isolated from patients with AIDS, AIDS related complex (ARC) and from healthy individuals at high risk for AIDS. Infection with HIV is followed by an acute flu-like illness. This phase may remain unnoticed and the relationship to HIV infection may not be clear in many cases. The acute phase is typically followed by an asymptomatic carrier state, which progresses to clinical AIDS in about 50% of infected individuals within 10 years after seroconversion. Serological evidence of infection with HIV may be obtained by testing for presence of HIV antigens or antibodies in serum of individuals suspected for HIV infection. Antigens can generally be detected during both acute phase and the symptomatic phase of AIDS only. The Antibodies to HIV-1 and/or HIV-2 can be detected throughout virtually the whole infection period, starting at, or shortly after the acute phase and lasting till the end stage of AIDS. Apart from sexual transmission, the principal route of infection with HIV is blood transfusion. HIV can present both in cellular and cell-free fractions of human blood. Therefore, all donations of blood or plasma should be tested due to the risk of HIV transmission through contaminated blood. The ELISA tests for detection of HIV infection are characterized with high sensitivity, specificity and simple operation procedure. There are most appropriate for testing of large numbers of specimens and currently, internationally available are hundreds of HIV tests used in routine blood screening or clinical diagnosis. Since the first HIV ELISA tests were commercially introduced in 1985, four more generations have been developed.

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