QIAseq FastSelect –rRNA Fly Kits

For rapid rRNA removal for RNA-seq library preparation from Drosophila melanogaster (fly) samples

Features

• Compatible with QIAGEN, Illumina, NEB and KAPA stranded RNA-seq library kits
• Single reagent for Drosophila melanogaster (fly) samples
• High-performance rRNA and/or globin removal in just 14 minutes
• Only one pipetting step – combine QIAseq FastSelect reagent with RNA and incubate
• No extra cleanup steps or NGS library protocol changes

Useful Resources

Products

QIAseq FastSelect –rRNA Fly Kits are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.
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QIAseq FastSelect –rRNA Fly Kit (24)

Cat. No. / ID: 333262

For 24 reactions: cytoplasmic and mitochondrial rRNA removal reagent; supports fly
€1,098.00
Add to cart
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QIAseq FastSelect –rRNA Fly Kit (96)

Cat. No. / ID: 333265

For 96 reactions: cytoplasmic and mitochondrial rRNA removal reagent; supports fly
€3,956.00
Add to cart

Product Details

QIAseq FastSelect –rRNA Fly Kits use a novel method to remove highly abundant RNA that is of low scientific value from your RNA-seq libraries. Researchers using RNA-seq for whole transcriptome analysis can use QIAseq FastSelect –rRNA Fly Kits to remove all annotated rRNAs in RefSeq and Ensembl for Drosophila melanogaster (fly). Depending on rRNA sequence homology, QIAseq FastSelect −rRNA Fly will work on additional fly species (dependent upon target rRNA sequence homology with D. melanogaster).
We recommend using QIAseq Stranded RNA Library Kits for robust strand-specific RNA-seq library preparation for high-quality and highly fragmented (FFPE) RNA. QIAseq Stranded RNA Library Kits utilize unique dual indexing (UDIs) which enables multiplexing of up to 384 samples per flow cell lane on Illumina NGS instruments and mitigates index hopping on Illumina NovaSeq and Illumina patterned flow cells.
Design your own custom QIAseq FastSelect pools to remove any RNAs you wish from your RNA-seq library – take a look at our QIAseq FastSelect Custom RNA Removal Kits .

Performance

QIAseq FastSelect –rRNA Fly Kits provide highly efficient removal of rRNA (figure QIAseq FastSelect –rRNA Fly Kits provide highly efficient removal of rRNA) and consistent read mapping (figures QIAseq FastSelect –rRNA Fly exon/intron/intergenic mapping, QIAseq FastSelect ‒rRNA Fly dramatically shifts read allocation from rRNA to genes and QIAseq FastSelect ‒rRNA Fly dramatically shifts read allocation from rRNA to genes: bar chart).

Principle

Removing highly expressed, but biologically unimportant RNA transcripts makes NGS more efficient and enables higher sample throughput with higher sensitivity. Furthermore, removal of unwanted RNA species from full length and fragmented RNA samples can be particularly challenging and can result in suboptimal performance.

QIAseq FastSelect –rRNA Fly Kits are designed for quick, efficient removal of cytoplasmic and mitochondrial fly ribosomal RNA from total RNA during NGS RNA library preparation. QIAseq FastSelect seamlessly integrates with your existing RNA stranded library preparation workflow for RNA removal in a single, 14-minute inline step. Prior to RNA heat fragmentation (which is optional and dependent upon the library preparation kit and sample type), QIAseq FastSelect removal reagent is directly combined with total RNA and the library preparation-specific buffers. After fragmentation, the reaction temperature is stepwise cooled to room temperature and the remaining library preparation steps are completed. There is no need to perform any type of enrichment on the total RNA samples. QIAseq FastSelect –rRNA Fly Kits ensure consistently high performance with RNA amounts ranging from as little as 1 ng up to 1 μg. QIAseq FastSelect can be used with RNA from fresh samples from many species of fly (dependent upon target rRNA sequence homology with D. melanogaster), and delivers reliable rRNA removal and high reproducibility in downstream applications.

Procedure

Most RNA removal or depletion strategies associated with RNA-seq library construction are sample pre-treatment strategies involving hybrid-capture or enzymatic removal of unwanted RNA. Our unique QIAseq FastSelect procedure is compatible with QIAGEN, Illumina, KAPA and NEB and other RNA library kits and provides complete rRNA removal in a single, 14-minute inline step (see figure  QIAseq FastSelect Kit workflow ). This is dramatically faster than alternative RNA depletion kits, which require pre-treatment protocols involving more than 25 steps and 2 hours to complete.

Simply add QIAseq FastSelect reagent to the RNA sample, perform fragmentation (if required), stepwise cool the reaction from 75°C to 25°C for 14 minutes and then complete the remaining library preparation steps. QIAseq FastSelect works with or without RNA fragmentation, providing the flexibility to use fragmented RNA from fly samples or high-quality RNA as part of a standard RNA-seq library construction workflow.

See figures

Applications

QIAseq FastSelect delivers rapid, reliable RNA removal from full length or fragmented RNA samples from many species of fly (dependent upon target rRNA sequence homology with D. melanogaster). QIAseq FastSelect –rRNA Fly Kits are available in a variety of different formats and sizes to suit your specific applications.

Supporting data and figures

Resources

Kit Handbooks (1)

Publications

Exercise-induced functional desensitization of canine cardiac beta-adrenergic receptors.
Friedman DB; Ordway GA; Williams RS;
J Appl Physiol (1985); 1987; 62 (4):1721-3 1987 Apr PMID:3036756
Balancing precision versus cohort transcriptomic analysis of acute and recovery phase of viral bronchiolitis.
Gupta R; Leimanis ML; Adams M; Bachmann AS; Uhl KL; Bupp CP; Hartog NL; Kort EJ; Olivero R; Comstock SS; Sanfilippo DJ; Lunt SY; Prokop JW; Rajasekaran S;
Am J Physiol Lung Cell Mol Physiol; 2021; 320 (6):L1147-L1157 2021 Apr 14 PMID:33851876