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Viruses take lives. Early, accurate detection and differentiation is the first step to proper treatment.
The arrival of COVID-19 into the ecosystem changed the way we approach respiratory testing. Gone are the days or relying on a rapid test to diagnose an infection. PCR or molecular testing is now the gold standard. Its magnifying capacity allows laboratorians to detect the virus, even when there are minimal copies in the host
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Internal control |
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Authorized sample types |
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Turnaround time from sample to interpreted results is approximately 3 hours. The required workflow consists of sample extraction and preparation, real-time RT-PCR genetic analysis, and automated translation of data into patient diagnosis.
The Applied Biosystems Pathogen Interpretive Software EUA Edition is part of the required workflow and must be downloaded prior to instrumentation use.
You may download the software upon kit purchase. Labs following the authorized workflow are required to complete an eLearning course and pass an exam to download.
Follow the instructions below to obtain the software from your local support team:
Product | Included component | Qty | Cat. No. |
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TaqPath COVID-19, Flu A, Flu B Combo Kit | TaqPath COVID-19, Flu A, Flu B RT-PCR Assay (1 tube) | 1,000 rxns | |
MS2 Phage Control (10 tubes) | |||
TaqPath COVID-19, Flu A, Flu B Control Kit (10 tubes) | |||
TaqPath COVID-19 Control Dilution Buffer (10 tubes) |
Find the approved Instructions for Use (IFU) for your country. (Note: Product availability varies by country.)