Hologic panther pcr
General Information Panther Fusion® SARS-CoV-2 SARS-CoV-2 - Panther Fusion System 2 AW-21159-001 Rev. 004 General Information Intended Use The Panther Fusion® SARS-CoV-2 assay is a real-time RT-PCR in vitro diagnostic test intended for the qualitative detection of RNA from SARS-CoV-2 isolated and purified from upperPanther System Molecular Testing High … Add the Panther system to your lab and the capability to consolidate menu on a fully automated system, load samples in any order at any time, eliminate batch constraints and decrease turnaround time; The Aptima® assays help guide patient care and enable earlier detection
Hologic’s current diagnostic offering is anchored by the Panther ® System, a best-in-class, fully automated, sample-to-result platform designed to be used across laboratories of varying ... The Panther Fusion system adds PCR (polymerase chain reaction) chemistry and provides an expanded in vitro diagnostics menu, as well as Open Access functionality to run laboratory developed tests. Together, the Panther and Panther Fusion systems now offer 16 FDA-cleared assays and 20 CE-marked assays that detect more than 20 pathogens.This study compared three of these assays, the Hologic Panther Fusion SARS-CoV-2 assay (Fusion), the Hologic Aptima SARS-CoV-2 assay (Aptima), and the BioFire Defense COVID-19 test (BioFire), to determine analytical and clinical performance as well as workflow.AIDS rapid diagnostic test Aptima HIV-1 RNA qualitative assay. HIV serum plasma. cervical cancer rapid diagnostic test Aptima HPV assay. HPV. sexually transmitted disease rapid diagnostic test Aptima Trichomonas vaginalis assay. cervical cancer rapid diagnostic test Cervista HPV 16/18 assay. HPV.
Feb 04, 2021 · PCR tests are highly accurate, but slow. Rapid antigen tests are, well, rapid, but aren't as sensitive. The Hologic Panther system is the best of both worlds, MacMillan said. Table 3. FDA-cleared Nucleic Acid Detection Based Tests for Influenza Viruses 1. Mesa Biotech. Inc. Seasonal Flu A/H3N2, A/H1N1pdm09, and Non-seasonal Influenza A subtypes (i.e., not A/H3N2 or A/H1N1pdm09). B/Victoria and B/Yamagata. Available FDA cleared tests as of August 2020.