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Hiv 1 2 unigold recombinant assay

Manufactured by Trinity Biotech
Sourced in Ireland

The HIV-1/2 Unigold Recombinant Assay is a rapid diagnostic test that detects antibodies to HIV-1 and HIV-2 in human serum, plasma, or whole blood samples. The test utilizes recombinant HIV-1 and HIV-2 antigens to identify the presence of HIV-specific antibodies in the sample.

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2 protocols using hiv 1 2 unigold recombinant assay

1

Tuberculosis Screening and Diagnosis in Prisons

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For each participant with a positive cough screen, spot and morning sputum samples were collected in the prison health clinic. Acid-fast bacilli (AFB) smear microscopy was performed with regular light microscopy using the Ziehl-Neelsen (ZN) technique.24 The remaining portions of the samples were transported daily in ice boxes to the regional public health laboratory, which was about 500 m away. The two sputum samples were pooled in a single container and stored at −20°C until transport to Armauer Hansen Research Institute (AHRI) in Addis Ababa.
External quality control was performed for all slides by an independent, experienced laboratory technician at AHRI who was blinded to the AFB microscopy and Xpert results.
HIV screening was performed according to the national testing algorithm. Briefly, blood samples from finger-pricks were tested first with HIV (1+2) Antibody Colloidal Gold (Shanghai Kehua Bioengineering, Shanghai, China); positive samples were confirmed using Stat-Pak (Chembio, Medford, Brookhaven, NY, USA), while discordant results were resolved using HIV-1/2 Unigold Recombinant Assay (Trinity Biotech, Bray, Ireland).
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2

Validated HIV Testing Regimen in Ethiopia

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HIV test was done by a tiebreaker regimen consisting of three rapids HIV (1 + 2) tests in the hospital following the national algorithm recommend by the Federal Ministry of Health [20] . HIV (1 + 2) Antibody Colloidal Gold (KHB, Shanghai Kehua Bio-engineering Co Ltd, China) test is run first on whole blood , and any positive samples are then confirmed using the second test (HIV 1/2 STAT-PAK (Chembio Diagnostics, USA). Any discordant results were resolved using a third confirmatory testing kit, HIV-1/2 Unigold Recombinant assay (Trinity Biotech, Ireland). Invalid tests where the control line did not appear were discarded and repeated on new test devices according to manufacturers’ instructions.
The HIV test was processed following manufacturers’ instructions and Institutional Standard Operation Procedure. The quality of each kits used for HIV test was validated using known HIV positive and negative stored serum in the center. The performance of the diagnostic center was monitored by the Gambella Regional Laboratory and Ethiopia National HIV/AIDS Reference Laboratory though on site periodical supervision and sending blind Panel Test with known result.
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