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Status |
Public on Dec 05, 2014 |
Title |
Complex in vivo RNA-seq analysis reveal reprogramming of Yersinia from virulent to persistent mode during infection [microarray I] |
Platform organism |
Yersinia pseudotuberculosis |
Sample organism |
Yersinia pseudotuberculosis YPIII |
Experiment type |
Expression profiling by array
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Summary |
Whole transcriptome assessment of the Yersinia pseudotuberculosis strain YPIII grown under aerobic or anaerobic conditions to exponential phase.
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Overall design |
Y. pseudotuberculosis YPIII was grown at 25°C in LB medium supplemented with 10 g/l glucose and 0.2 M HEPES buffer under aeration or under anaerobic growth conditions (in a nitrogen atmosphere) on a rotary shaker. Total RNA was extracted using SV Total RNA Isolation System (Promega). The samples were treated with RNase-free DNase (Roche Applied Science) and the quality of the RNA was confirmed by the lack of PCR amplification of the hns gene and by using an Agilent 2100 Bioanalyzer.
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Contributor(s) |
Heroven AK, Beckstette M, Dersch P |
Citation missing |
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Submission date |
Apr 02, 2014 |
Last update date |
Dec 06, 2014 |
Contact name |
Kemal Avican |
E-mail(s) |
kemal.avican@umu.se
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Organization name |
Umea University
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Department |
Department of Molecular Biology
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Lab |
Maria Fällman's Lab
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Street address |
Building 6L
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City |
Umea |
ZIP/Postal code |
90187 |
Country |
Sweden |
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Platforms (1) |
GPL15095 |
Agilent-020412 Yersinia pseudotuberculosis YPIII gene expression array |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE56477 |
Complex in vivo RNA-seq analysis reveal reprogramming of Yersinia from virulent to persistent mode during infection |
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Relations |
BioProject |
PRJNA243388 |