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Qubit br dsdna kit

Manufactured by Agilent Technologies

The Qubit BR dsDNA kit is a fluorescence-based assay designed to quantify double-stranded DNA (dsDNA) samples. The kit utilizes a fluorescent dye that binds specifically to dsDNA, allowing for accurate measurement of DNA concentration.

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2 protocols using qubit br dsdna kit

1

Rapid SARS-CoV-2 Genome Sequencing Workflow

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total RNA was isolated from VTM within 72 hours of specimen collection using the Omega Bio-Tek Viral RNA Xpress kit (Norcross, GA) on an automated extraction platform. Presence of SARS-CoV-2 RNA was determined by using CDC primers and probes with LunaScript RT Supermix Kit (NEB) run on BioRad (Hercules, CA) C1000 real-time PCR machines. cDNA, PCR amplification, and library preparation was performed using the NEBNext ARTIC SARS-CoV-2 FS kit (NEB) according to the manufacturer’s instructions. Libraries were quantified using Invitrogen Qubit BR dsDNA kit and size determined on an Agilent Tapestation 2200 using high sensitivity d1000 tapes (Santa Clara, CA). Libraries were loaded at 10.5 pM on an Illumina (San Diego, CA) MiSeq version 2, 300 cycle kit on an Illumina MiSeq instrument. Consensus sequences were generated with an in-house data analysis pipeline using bwa, samtools, and ivar.
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2

Rapid SARS-CoV-2 Genome Sequencing Workflow

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total RNA was isolated from VTM within 72 hours of specimen collection using the Omega Bio-Tek Viral RNA Xpress kit (Norcross, GA) on an automated extraction platform. Presence of SARS-CoV-2 RNA was determined by using CDC primers and probes with LunaScript RT Supermix Kit (NEB) run on BioRad (Hercules, CA) C1000 real-time PCR machines. cDNA, PCR amplification, and library preparation was performed using the NEBNext ARTIC SARS-CoV-2 FS kit (NEB) according to the manufacturer’s instructions. Libraries were quantified using Invitrogen Qubit BR dsDNA kit and size determined on an Agilent Tapestation 2200 using high sensitivity d1000 tapes (Santa Clara, CA). Libraries were loaded at 10.5 pM on an Illumina (San Diego, CA) MiSeq version 2, 300 cycle kit on an Illumina MiSeq instrument. Consensus sequences were generated with an in-house data analysis pipeline using bwa, samtools, and ivar.
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