|
Status |
Public on Mar 08, 2012 |
Title |
mRNA degradation in Mycobacterium tuberculosis under aerobic conditions |
Organism |
Mycobacterium tuberculosis H37Rv |
Experiment type |
Other
|
Summary |
Transcription was arrested using 50 ug/ul of rifampin leaving RNA degradation as the sole vector responsible for mRNA abundance. mRNA half-lives were calculated from the decay of signal intensity from T0.
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Overall design |
Four replicates were sampled after 0, 5 10, 15, 20, and 30 minutes of mRNA decay for a total of 24 arrays.
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Contributor(s) |
Rustad T, Brabant W |
Citation(s) |
23125364 |
|
Submission date |
Mar 07, 2012 |
Last update date |
Feb 19, 2013 |
Contact name |
Tige Rustad |
E-mail(s) |
tige.rustad@sbri.org
|
Phone |
206-256-7207
|
Organization name |
Seattle Biomedical Research Institute
|
Department |
Pathobiology
|
Lab |
Sherman
|
Street address |
307 Westlake Avenue N, Suite 500
|
City |
Seattle |
State/province |
WA |
ZIP/Postal code |
98109 |
Country |
USA |
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Platforms (1) |
GPL14824 |
SBRI_MTuberculosis_12x130K_ver2.0 |
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Samples (24)
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This SubSeries is part of SuperSeries: |
GSE36345 |
mRNA degradation in Mycobacterium tuberculosis |
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Relations |
BioProject |
PRJNA155557 |