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oraquick ebola rapid antigen test  (OraSure Inc)

 
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    OraSure Inc oraquick ebola rapid antigen test
    Oraquick Ebola Rapid Antigen Test, supplied by OraSure Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/oraquick ebola rapid antigen test/product/OraSure Inc
    Average 90 stars, based on 1 article reviews
    oraquick ebola rapid antigen test - by Bioz Stars, 2026-03
    90/100 stars

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    Sensitivity performance of the OraQuick ® Ebola Rapid Antigen Test.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Sensitivity performance of the OraQuick ® Ebola Rapid Antigen Test.

    Article Snippet: The OraQuick ® Ebola Rapid Antigen Test (OraSure Technologies, Inc., Bethlehem, PA, USA) was selectively used to test directly collected cadaver oral fluid samples obtained from Sierra Leone, Guinea, and Liberia, as it was the only RDT approved to detect the EBOV in contrived saliva samples.

    Techniques: Virus, Irradiation

    Ebola Rapid Antigen Test agreement compared to the CDC Ebola Virus VP40 rRT-PCR Assay.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Ebola Rapid Antigen Test agreement compared to the CDC Ebola Virus VP40 rRT-PCR Assay.

    Article Snippet: The OraQuick ® Ebola Rapid Antigen Test (OraSure Technologies, Inc., Bethlehem, PA, USA) was selectively used to test directly collected cadaver oral fluid samples obtained from Sierra Leone, Guinea, and Liberia, as it was the only RDT approved to detect the EBOV in contrived saliva samples.

    Techniques: Virus

    Assay performance summary for the OraQuick ® assay using venous and fingerstick NHP blood compared to the EZ1 RT-PCR assay.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Assay performance summary for the OraQuick ® assay using venous and fingerstick NHP blood compared to the EZ1 RT-PCR assay.

    Article Snippet: The OraQuick ® Ebola Rapid Antigen Test (OraSure Technologies, Inc., Bethlehem, PA, USA) was selectively used to test directly collected cadaver oral fluid samples obtained from Sierra Leone, Guinea, and Liberia, as it was the only RDT approved to detect the EBOV in contrived saliva samples.

    Techniques: Biomarker Discovery

    Detection of inactive viruses from the genus Ebolavirus with Ebola Rapid Antigen Test in whole blood.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Detection of inactive viruses from the genus Ebolavirus with Ebola Rapid Antigen Test in whole blood.

    Article Snippet: The OraQuick ® Ebola Rapid Antigen Test (OraSure Technologies, Inc., Bethlehem, PA, USA) was selectively used to test directly collected cadaver oral fluid samples obtained from Sierra Leone, Guinea, and Liberia, as it was the only RDT approved to detect the EBOV in contrived saliva samples.

    Techniques: Virus, Concentration Assay

    Sensitivity performance of the OraQuick ® Ebola Rapid Antigen Test.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Sensitivity performance of the OraQuick ® Ebola Rapid Antigen Test.

    Article Snippet: The OraQuick ® Antigen Ebola Rapid Antigen Test and DPP Ebola Antigen System (Chembio Diagnostic Systems, Inc.) are the only two rapid tests with FDA EUA authorization; however, the EUA approvals were phased out with the OraQuick ® 510(k) clearance.

    Techniques: Virus, Irradiation

    Ebola Rapid Antigen Test agreement compared to the CDC Ebola Virus VP40 rRT-PCR Assay.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Ebola Rapid Antigen Test agreement compared to the CDC Ebola Virus VP40 rRT-PCR Assay.

    Article Snippet: The OraQuick ® Antigen Ebola Rapid Antigen Test and DPP Ebola Antigen System (Chembio Diagnostic Systems, Inc.) are the only two rapid tests with FDA EUA authorization; however, the EUA approvals were phased out with the OraQuick ® 510(k) clearance.

    Techniques: Virus

    Assay performance summary for the OraQuick ® assay using venous and fingerstick NHP blood compared to the EZ1 RT-PCR assay.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Assay performance summary for the OraQuick ® assay using venous and fingerstick NHP blood compared to the EZ1 RT-PCR assay.

    Article Snippet: The OraQuick ® Antigen Ebola Rapid Antigen Test and DPP Ebola Antigen System (Chembio Diagnostic Systems, Inc.) are the only two rapid tests with FDA EUA authorization; however, the EUA approvals were phased out with the OraQuick ® 510(k) clearance.

    Techniques: Biomarker Discovery

    Detection of inactive viruses from the genus Ebolavirus with Ebola Rapid Antigen Test in whole blood.

    Journal: Viruses

    Article Title: Development and Clinical Evaluation of a Rapid Point of Care Test for Ebola Virus Infection in Humans

    doi: 10.3390/v15020336

    Figure Lengend Snippet: Detection of inactive viruses from the genus Ebolavirus with Ebola Rapid Antigen Test in whole blood.

    Article Snippet: The OraQuick ® Antigen Ebola Rapid Antigen Test and DPP Ebola Antigen System (Chembio Diagnostic Systems, Inc.) are the only two rapid tests with FDA EUA authorization; however, the EUA approvals were phased out with the OraQuick ® 510(k) clearance.

    Techniques: Virus, Concentration Assay