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SRX9518452: RNA-seq of Chilo suppressalis: midgut of 3rd instar larvae
1 ILLUMINA (Illumina HiSeq 4000) run: 15,658 spots, 22M bases, 5.4Mb downloads

Design: A total amount of 2 g RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext UltraTM RNA Library Prep Kit for Illumina (NEB, USA) following manufacturers recommendations and index codes were added to attribute sequences to each sample. Briefly, mRNA was purified from total RNA using poly-T oligo-attached magnetic beads. Fragmentation was carried out using divalent cations under elevated temperature in NEBNext First Strand Synthesis Reaction Buffer 5X. First strand cDNA was synthesized using random hexamer primer and M-MuLV Reverse Transcriptase RNase H. Second strand cDNA synthesis was subsequently performed using DNA Polymerase I and RNase H. Remaining overhangs were converted into blunt ends via exonuclease/polymerase activities. After adenylation of 3 ends of DNA fragments, NEBNext Adaptor with hairpin loop structure were ligated to prepare for hybridization. In order to select cDNA fragments of preferentially 200-250 bp in length, the library fragments were purified with AMPure XP system (Beckman Coulter, Beverly, USA). Then 3 l USER Enzyme (NEB, USA) was used with size-selected, adaptor-ligated cDNA at 37C for 15 min followed by 5 min at 95C before PCR. Then PCR was performed with Phusion High-Fidelity DNA polymerase, Universal PCR primers and Index (X) Primer. At last, PCR products were purified (AMPure XP system) and library quality was assessed on the Agilent Bioanalyzer 2100 system.
Submitted by: Institute of Plant Protection, Chinese Academy of Agricultural Sciences
Study: Chilo suppressalis Transcriptome or Gene expression
show Abstracthide Abstract
3rd instar larvae treated with Cry9A protein
Sample: Invertebrate sample from Chilo suppressalis
SAMN16812963 • SRS7726102 • All experiments • All runs
Library:
Name: Cs-mRNA
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Runs: 1 run, 15,658 spots, 22M bases, 5.4Mb
Run# of Spots# of BasesSizePublished
SRR1307093515,65822M5.4Mb2024-11-16

ID:
12438240

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