Тest system for detecting of RNA of coronavirus strain SARS-CoV-2 using reverse transcription PCR (RT-PCR)

 

The set is aimed for detecting of RNA of coronavirus of strain SARS-CoV-2 in biotic substrates and based on the principle of RT-PCR. The set is developed to detect genome SARS-CoV-2 paragraphs. The positive detection control consists of the synthetic RNA SARS-CoV-2 and should be amplified together with the analyzed samples.

Collection of samples

For detecting of RNA of coronavirus strain SARS-CoV-2 is possible to withdraw the following biological substrates:

  • Rhinopharynx mucosa swabs and/or oropharynx posterior wall swabs (in the presence of symptoms of the anatomical airway damage);
  • expectoration or bronchoalveolar lavage (in case of tracheal intubation);
  • blood plasma;
  • fecal matter (in the presence of GI tract damage symptoms).

Brief review of experimental record.

  1. To perform a general RNA extraction using a recommended extraction set
  2. To prepare and to pour out in the test tubes the working solution of reagent mixture, to add the samples
  3. To close the test-tubes, to put them into thermo cycler, to adjust and to set into action RТ-PCR
  4. Growth curves analysis in samples tested, control samples and identifying standards

 

Total time, necessary for finishing of RТ-PCR in accordance with this protocol is approximately 1 hour 30 minutes.

 

 


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