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Quantifluor rna sample system

Manufactured by Promega
Sourced in France

The QuantiFluor RNA Sample System is a fluorescent-based quantitation method for measuring RNA concentration. The system utilizes a fluorescent dye that binds to RNA, allowing for accurate and sensitive RNA quantification. The core function of the QuantiFluor RNA Sample System is to provide a reliable and efficient way to determine the concentration of RNA samples.

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2 protocols using quantifluor rna sample system

1

RNA Extraction and Sequencing of W. magna

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RNA extraction of W. magna c2c maky was carried out using the RNeasy Mini Kit (Qiagen, Hilden, Germany). The QuantiFluor RNA sample system (Promega) was used to quantify total RNA from each sample. Total RNA was qualified using Nano RNA chip on BioAnalyser 2100 (Agilent Technologies Inc.). A poly A capture was performed to purify mRNA from the total RNA. Libraries were then generated using NextFlex rapid directional RNAseq sample prep (Bioo Scientific Corporation). Libraries were quantified using dsDNA HS Assay on Quantus Fluorometer and qualified on BioAnalyser 2100 from Agilent using HS DNA chip. Sizes of fragments in the library were about 380 bp, therefore compatible with cluster generation. Paired-end sequencing with 75 bp read length was performed on NextSeq. 500 Mid Output flow cell lines from Illumina generating 130 million reads. The sequencing of two RNA samples generated 216.93 million of raw reads, 77.4% of which met the Illumina filtering criteria.
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2

Illumina Sequencing of Total RNA

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The total RNA of each sample was extracted using a RNeasy Mini Kit (Qiagen, Hilden, France) according to the manufacturer’s instructions. RNA was quantified and qualified using a QuantiFluor RNA sample system (Promega, Charbonnières, France) and a nano RNA chip on a BioAnalyser 2100 (Agilent Technologies Inc., Santa Clara, CA, United States), respectively. Illumina sequencing was performed using ProfileXpert/Viroscan3D, Lyon. Briefly, libraries were prepared from total RNA using poly(A) enrichment of the mRNA to remove ribosomal RNA. NextFlex rapid directional RNAseq sample prep (Bioo Scientific Corporation) was used to achieve the libraries. Quantification and validation of the libraries were performed using dsDNA HS Assay on a Quantus Fluorometer (Promega, Charbonnières, France) and on a BioAnalyser 2100 from Agilent using a HS DNA chip (Agilent Technologies Inc., Santa Clara, CA, United States), respectively. The library was sequenced in 75 base pair (bp) length paired end reads in NextSeq 500 Mid Output flow cell lines from Illumina (Illumina Inc, San Diego, CA, USA) generating 216.9 million raw read pairs.
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