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SRX22159492: GSM7851881: Myco Feriruminatoris 1_b; Mycoplasma feriruminatoris; RNA-Seq
1 ILLUMINA (NextSeq 2000) run: 12.3M spots, 1.3G bases, 372.9Mb downloads

External Id: GSM7851881_r1
Submitted by: Centre for Genomic Regulation
Study: Mycoplasma feriruminatoris transcriptome
show Abstracthide Abstract
The goal of this experiment is to determine the overall relative strength of promoter sequences in Mycoplasma feriruminatoris. For this, 2 replicates were grown in parallel in Hayflick media and the RNA wa extracted at exponential growth phase (20 hours). With this data, new promoter sequences could be designed and further validated by the use of RT-qPCR and reporter assays. Overall design: The cultures were started at 1:1000 proportion (10 µl in 10 ml of growth media). They were left to grow for 20 hours and collected at exponential phase. The cells were separated and washed via centrifugation. The cellular pellet was then extracted using a standard RNA extraction method using the RNeasy kit from Qiagen. The stage of exponential growth phase was confirmed via CFU/ml counting.
Sample: Myco Feriruminatoris 1_b
SAMN37909730 • SRS19218365 • All experiments • All runs
Library:
Name: GSM7851881
Instrument: NextSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Cells separated from supernatant by centrifugation at 10,000 rpm and washed 3 times in PBS 1x. Bacterial pellet treated with RLT buffer (Rneasy kit, Qiagen) supplemented with 1:100 beta-mercaptoethanol. The rest of the protocol was followed as per the manufacturer's instructions. RNA libraries were prepared for sequencing using standard Illumina protocols polyA-selected stranded RNA-seq
Runs: 1 run, 12.3M spots, 1.3G bases, 372.9Mb
Run# of Spots# of BasesSizePublished
SRR2645529612,316,7771.3G372.9Mb2024-05-08

ID:
30112927

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