Advanced assay design to compensate for emerging SARS-CoV-2 mutations

 

In order to provide increased confidence in our COVID-19 test results as SARS-CoV-2 continues to mutate, our TaqPath COVID-19 2.0 tests employ an advanced assay design with increased target redundancy to compensate for both currently known and future SARS-CoV-2 mutations.

Blog series: The Next Generation of COVID-19 Testing

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The new TaqPath assay designs cover three genomic regions and eight total targets.

This design is used across both of our TaqPath COVID-19 2.0 tests.

 

Product details

 

TaqPath COVID-19 2.0 assay details

CE-IVD Kit

Internal control

Sample type

Limit of detection

Turnaround time
(sample to result)

Approved sample
preparation

Approved system
and software

TaqPath COVID-19 Fast PCR Combo Kit 2.0

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RNase P

 

Raw saliva

750–1,000 GCE/mL*

~2 hours

Lysis (Applied Biosystems
SalivaReady Solution–
Assay design, included in the combo kit)

TaqPath COVID-19 RNase P Combo Kit 2.0

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  • Nasopharyngeal swab (NPS)
  • Anterior nasal (nasal) swab

75 GCE/mL**

 

~3 hours

Thermo Scientific KingFisher
Flex Purification System with

Applied Biosystems MagMAX
Viral/Pathogen II Nucleic Acid Isolation Kit

*LOD of 750 GCE/mL using QuantStudio 7 Flex instrument (384-well); LOD of 1,000 GCE/mL using QuantStudio 5 instrument (96-well, 0.2 mL). LOD was determined using pooled, contrived raw saliva samples that were spiked with gamma-irradiated SARS-CoV-2, Isolate USA-WA1/2020 (BEI Resources, PN NR-52287, LN 70033322).
** A bridging study yielded 100% positivity (20/20) at 1x LoD for the QuantStudio 5 Instrument (96-well, 0.2 mL)

 

Features

 

TaqPath COVID-19 2.0 test assays

Thermo Fisher Scientific continues to provide gold standard testing technology with our evolved PCR-based TaqPath COVID-19 2.0 tests, which were developed to help laboratories quickly diagnose COVID-19 caused by SARS-CoV-2 infection. 

Features of the TaqPath COVID-19 2.0 test assays:

  • Same accuracy and reliability you’ve grown to trust—An advanced assay design compensates for current and emerging mutations, helping provide continued confidence in results now and into the future
  • Multiple workflow options—Choose from 2 tests options: one utilizing a standard workflow that includes RNA extraction, and the second utilizing a fast, direct-to-PCR workflow with no RNA extraction required
  • Affordable and scalable—Add to your existing COVID-19 test menu using your current real-time PCR instrumentation
  • Easier storage—Store your TaqPath COVID-19 2.0 combo kits at -20°C

Find your IFU

Find the approved Instructions for Use (IFU) for your country. (Note: Product availability varies by country.)

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For In Vitro Diagnostic Use. Regulatory requirements vary by country. Product may not be available in your geographic region. © 2021 Thermo Fisher Scientific Inc.

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