DPP® HIV 1/2 Assay


dpp half screen assay1

Earlier Detection Table

Chembio has developed a NEXT GENERATION DPP® assay using patented DPP® technology for the rapid detection of HIV 1 and HIV 2 antibodies in oral fluid and all blood matrices. The Chembio DPP® HIV 1/2 Assay is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV 1 and HIV 2. This test is suitable for use in multi-test algorithms that have been established in many countries or as a standalone initial test.

* Consult product insert for interpretation of results

For Use With:

  • Oral fluid sample
  • Venipuncture whole blood
  • Serum
  • Plasma
  • Fingerstick whole blood

Assay Features:

  • Sharp & distinctive visual results
  • Excellent sensitivity and specificity
  • Built-in procedural control to human IgG
  • DPP®SampleTainer® bottle: a safe, closed system for handling potentially infectious blood and oral fluid samples

Convenient & Cost Effective

  • Ideally suited for field and point-of-care testing
  • Minimal sample size required — 10 µL
  • Room temperature storage and procedure
  • Ready-to-use reagents
  • 24-month open vial stability for quality controls — 50 control runs per vial
  • Long shelf life (24 months from date of manufacture)
  • No special laboratory equipment required
Catalog Number
DPP® HIV 1/2 Assay, FDA Approved
20 - Individually Pouched DPP® HIV 1/2 Test Devices with Desiccant pouch
1 - Quick Reference Instructions (for CLIA Waived)
20 - Copies of Subject Information Notice
20 - Oral Fluid Swabs
20 - Disposable 10μL Sample Loops
20 - DPP SampleTainer® bottle - BLACK Cap
1 - DPP HIV Running Buffer - GREEN Cap
1 - Product Insert for the DPP HIV 1/2 Assay
DPP® HIV 1/2 Rapid Test Control Pack
1 pack contains:
-1 HIV-1 Reactive Control 0.5 mL
-1 HIV-2 Reactive Control 0.5 mL
-1 HIV Nonreactive Control 0.5 mL
Each kit control vial contains sufficient volume to run 50 tests

Contact our sales department

Call: 1-844-CHEMBIO (844-243-6246); Outside the U.S. 1-631-924-1135
Email: customerservice@chembio.com

FDA Approved CLIA waived for Oral Fluid, Fingerstick and Venous Whole Blood

U.S. Reimbursement Code: 86703-QW, G0435-QW, G0433-QW*

*The information provided is general reimbursement information only. It is neither legal nor coding advice. It is the responsibility of the provider to contact its carrier/payer for official coding and coverage policies.