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SRX13653995: GSM5776709: krrA 205-3; Bacillus anthracis; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 26.6M spots, 8G bases, 2.5Gb downloads

External Id: GSM5776709_r1
Submitted by: VUMC
Study: A Bacillus anthracis RNA binding protein post-transcriptionally regulates two component signaling through RNA turnover [RNA-Seq]
show Abstracthide Abstract
To uncover the effects of KrrA regulation on gene transcription and define the bacterial response imposed by this regulation, a transcriptomic study was carried out in which Bacillus anthracis ?krrA was compared to WT in two growth conditions: LB in the presence or absence of '205. Overall design: Two strains of Bacillus anthracis (WT and krrA deletion mutant) in the presence or absence of 50 µM '205 were compared. RNA was isolated from each of the strains and conditions in triplicte and RNA sequencing performed. Transcriptomes and changes in expression patters were compared across each samples using CLC genomics workbench.
Sample: krrA 205-3
SAMN24720674 • SRS11539983 • All experiments • All runs
Library:
Name: GSM5776709
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total bacterial RNA was isolated utilizing the Qiagen RNeasy mini kit. DNA was removed by treatment with Invitrogen TURBO Dna-free kit and rRNA was depleted using the Invitrogen RiboMinus Transcriptome Isolation kit (bacteria) and the RiboMinus Concentration Module Library construction was performed using NEBNext Ultra II RNA Library Prep Kit for Illumina and NEBNext Multiplex Oligos for Illumina
Runs: 1 run, 26.6M spots, 8G bases, 2.5Gb
Run# of Spots# of BasesSizePublished
SRR1748347126,611,3648G2.5Gb2022-01-10

ID:
18989545

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