Selected article for: "nuclease free water and thermal cycling"

Author: Stefania Marzinotto; Catia Mio; Adriana Cifu'; Roberto Verardo; Corrado Pipan; Claudio Schneider; Francesco Curcio
Title: A streamlined approach to rapidly detect SARS-CoV-2 infection, avoiding RNA extraction
  • Document date: 2020_4_11
  • ID: mi6w8ppe_6
    Snippet: (which was not peer-reviewed) The copyright holder for this preprint DTT, 20U/µL Reverse Transcriptase, 5 µL sample and nuclease-free water were mixed and brought to a total volume of 20 µL. Samples were mixed with Droplet Generator Oil for Probes (Bio-Rad, catalog number 1863005) and droplets were generated on the automated droplet generator QX200™ Droplet Generator (Bio-Rad). PCR amplification was performed by the Veriti® Thermal Cycler (.....
    Document: (which was not peer-reviewed) The copyright holder for this preprint DTT, 20U/µL Reverse Transcriptase, 5 µL sample and nuclease-free water were mixed and brought to a total volume of 20 µL. Samples were mixed with Droplet Generator Oil for Probes (Bio-Rad, catalog number 1863005) and droplets were generated on the automated droplet generator QX200™ Droplet Generator (Bio-Rad). PCR amplification was performed by the Veriti® Thermal Cycler (ThermoFisher Scientific) with annealing at 55°C and standard thermal cycling conditions. Droplets were read on the QX200™ Droplet Reader (Bio-Rad) and reactions with less than 10'000 droplets were repeated. Data were analyzed using the QuantaSoft™ 1.7.4 Software (Bio-Rad).

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