Lateral Flow Immunoassay (LFI) > Maxim SwiftTM HIV Recent Infection Assay (RIA) Kit


    Catalog Number: 92002

    Components Included:
  • (20) Vials of Running Buffer in Sample Tube
  • (20) Test Cassettes sealed in a foil pouch
  • (23) 2 µL Capillary Transfer Pipette for Serum/ Plasma Samples (Clear Bag)
  • (23) 5 µL Capillary Transfer Pipette for Blood Samples (Pink Bag)

The Maxim SwiftTM HIV Recent Infection Assays are available in kits of 20 Tests

Order Hotline:
301-251-0800 ext. 10627
Service Hotline:
301-251-0800 ext. 10639
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Specification


Description:

The Maxim SwiftTM HIV Recent Infection Assay (RIA) is a single use qualitative immunoassay to detect the circulating antibodies to Human Immunodeficiency Virus Type 1 (HIV-1), Type 2 (HIV-2) and distinguish between recent and long-term infection in HIV-1. The assay is a point of care (POC) test intended for use with blood or serum/ plasma specimens.

The Maxim SwiftTM HIV RIA uses US CDC developed materials and is designed for surveillance purposes such as estimating HIV-1 incidence in a population, monitoring and evaluating HIV intervention programs, and recognizing those high-incidence populations so that prevention research, vaccine trials, and resources are most appropriately utilized.

This product is for research use only and is not intended for use in diagnostic procedures.

Related Products

Lateral Flow Immunoassay (LFI)

Maxim SwiftTM HIV Recent Infection Assay (RIA) Controls Kit - 92002-C

The Maxim SwiftTM HIV Recent Infection Assay (RIA) Kit Controls are quality control reagents for use only with the Maxim SwiftTM HIV Recent Infection Assay (RIA) (P/N 92002). They are used to verify that the test kit reagents are working and that the test is performed correctly.

Full Product Information

Description:

The Maxim SwiftTM HIV Recent Infection Assay (RIA) is a single use qualitative immunoassay to detect the circulating antibodies to Human Immunodeficiency Virus Type 1 (HIV-1), Type 2 (HIV-2) and distinguish between recent and long-term infection in HIV-1. The assay is a point of care (POC) test intended for use with blood or serum/ plasma specimens.

The Maxim SwiftTM HIV RIA uses US CDC developed materials and is designed for surveillance purposes such as estimating HIV-1 incidence in a population, monitoring and evaluating HIV intervention programs, and recognizing those high-incidence populations so that prevention research, vaccine trials, and resources are most appropriately utilized.

This product is for research use only and is not intended for use in diagnostic procedures.

Additional Information:

Product Insert
Video Tutorial
Step-by-Step Procedure
Swift HIV RIA Data Form

Product Inquiries

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Order Hotline: +1-301-251-0800 ext. 10627

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