Fighting the Syphilis and HIV Epidemics: Voices from the Field – NCSD Webinar
CE-Marked
FDA Approved
A dual rapid test for the detection of antibodies to HIV 1/2 and Treponema pallidum in fingerstick whole blood, venous whole blood, serum or plasma specimens.
Platform | Immunochromatographic Assay |
Format | Cassette |
Detection | HIV-1 and HIV-2 antibodies |
Specimen | Whole blood, serum & plasma |
Assay Time | 15 minutes |
Shelf Life* | 24 months |
*From date of manufacture
Description Title
Chembio’s proprietary DPP® technology differs from classical lateral flow tests by operating in a manner similar to that of the sequential ELISA format which is not sensitive to the “Hook Effect”.
DPP® Technological Advantages:
For Technical Support please call
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To contact your local state/territory health department click on the following link:
https://www.health.gov.au/about-us/contact-us/local-state-and-territory-health-departments
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