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Rt qpcr taqman assay

Manufactured by Integrated DNA Technologies

The RT-qPCR TaqMan assay is a molecular biology technique used for the detection and quantification of specific RNA sequences. It combines reverse transcription and real-time polymerase chain reaction (qPCR) to enable the amplification and measurement of target RNA molecules.

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2 protocols using rt qpcr taqman assay

1

SARS-CoV-2 Detection and Transcriptome Analysis

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We used residual NP samples remaining after clinical testing for CXCL10 measurements and transcriptome analysis. Swab-associated viral transport medium was stored at −80°C following clinical testing and thawed just before ELISA assay or RNA isolation for RNA-seq. Clinical information, including age, sex, virology results, and specific features of clinical course (including presenting symptoms, hospital admission, and length of stay), was extracted from the electronic medical record and recorded, after which samples were assigned a study code and deidentified. In the clinical laboratory, SARS-CoV-2 was detected in most samples using an Emergency Use Authorization–approved TaqMan assay detecting the CDC targets N1, N2, and RNaseP (Centers for Disease Control and Prevention, 2020 ). In some longitudinal samples, SARS-CoV-2 was diagnosed with the commercial Cepheid assay (Cepheid, 2021 ); in this case, RT-qPCR for the CDC N1 gene was repeated using RT-qPCR TaqMan assay for the CDC N1 gene as described previously (catalog no. 10006600; Integrated DNA Technologies; Vogels et al., 2020 (link)).
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2

SARS-CoV-2 Detection and Transcriptome Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
We used viral residual nasopharyngeal (NP) samples remaining after clinical testing for CXCL10 measurements and transcriptome analysis. Swab-associated viral transport medium was stored at −80 °C following clinical testing and thawed just prior to ELISA assay or RNA isolation for RNA-Seq. Clinical information including age, sex, virology results, and specific features of clinical course including presenting symptoms, hospital admission and length of stay, was extracted from the electronic medical record and recorded, after which samples were assigned a study code and de-identified. In the clinical laboratory, SARS-CoV-2 was detected in most samples using an EUA-approved TaqMan assay detecting the CDC targets N1, N2, and RNAseP (Prevention, 2020 ). In some longitudinal samples, SARS-CoV-2 was diagnosed with the commercial Cepheid assay (reference); in this case, RT-qPCR for the CDC N1 gene was repeated using RT-qPCR TaqMan assay for the CDC N1 gene as described previously (Cat no: 10006600, Integrated DNA Technologies, IA)(Vogels et al., 2020 (link)).
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