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SRX21980357: SHAPE-Seq of telomerase RNA Physcomitrium Patens
1 ILLUMINA (NextSeq 500) run: 795,307 spots, 240.2M bases, 96.4Mb downloads

Design: 10 pmol of in vitro transcribed RNA was denatured at 95 C for 2 minutes, quickly cooled down on the ice, mixed with a folding buffer (333 mM HEPES, pH 8.0; 333 mM NaCl; 33 mM MgCl2) and folded at 37 C for 20 minutes. This RNA was used for the modification reactions with 100 mM 1M7 (Sigma Aldrich) (+), DMSO (-), and DC (denaturing control). Modified RNAs prepared in triplicates were purified with SPRI beads and used for reverse transcription with Superscript-II in the presence of MnCl2 (SHAPE-Seq).
Submitted by: Central European Institute of Technology, Masaryk University
Study: Single molecule analysis reveals functionally relevant isoforms of telomerase RNA in moss
show Abstracthide Abstract
The goal of the study is to determine the secondary structure of telomerase RNA in P. patens in vivo (using DMS-Seq) or in vitro (using SHAPE-Seq). cDNA with induced mutations was generated with TGIRT-II or Superscript-II in the presence of MnCl2 (SHAPE-Seq). Samples for sequencing were prepared in biological triplicates.
Sample:
SAMN37642559 • SRS19055625 • All experiments • All runs
Library:
Name: T7_1M7_DC_3
Instrument: NextSeq 500
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: RT-PCR
Layout: PAIRED
Runs: 1 run, 795,307 spots, 240.2M bases, 96.4Mb
Run# of Spots# of BasesSizePublished
SRR26270850795,307240.2M96.4Mb2024-01-01

ID:
29888637

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