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Status |
Public on Feb 24, 2016 |
Title |
ΔaceA PQ 1mM 2 |
Sample type |
RNA |
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|
Source name |
PQ 1mM
|
Organism |
Pseudomonas aeruginosa PAO1 |
Characteristics |
strain: ΔPA2634 transposon insertion mutant treatment: 1mM PQ
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Treatment protocol |
Exponential phase cell was used for microarray analysis. In case of paraquat treatment, 1mM concentration of paraquat was added on exponential phase cell for 15min.
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Growth protocol |
Overnight culture was diluted 1:100 in 5 mL LB medium at 37°C with aeration.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA extracted using Trizol following manufacturer's instructions
|
Label |
Cy5
|
Label protocol |
Labeling reactions were performed with a Bioprime labeling kit (Invitrogen) in a volume of 50 μl with a modified dNTP pool containing 120 μM each of dATP, dGTP, and dCTP; 60 μM dTTP; and 60 μM Cy5-dUTP (for all)
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Hybridization protocol |
Labeled cDNAs were mixed with hybridization solution (MYcroarray.com), and the hybridization mixtures were heated at 65℃ for 5 min and then immediately cooled on ice for 5 min. Hybridization mixtures were directly loaded onto assembled MYcroarray.com microarray. The arrays hybridized at 50℃ for 16 hr using Agilent Hybridization oven (Agilent Technology, USA).
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Scan protocol |
The hybridization images were analyzed by GenePix Pro 6.0 (Axon Instruments, CA).
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Data processing |
The average fluorescence intensity for each spot was calculated and local background was subtracted. All data normalization and selection of fold-changed genes were performed using GenoWiz 4.0 (Ocimumbiosolutions, India).
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Submission date |
Feb 23, 2016 |
Last update date |
Feb 24, 2016 |
Contact name |
Sungeun Ahn |
E-mail(s) |
[email protected]
|
Organization name |
Korea university
|
Department |
molecular microbiology
|
Lab |
molecular environmental microbiology Laboratory
|
Street address |
Anamro
|
City |
Anam-Dong, Seungbuk-Ku |
State/province |
Seoul |
ZIP/Postal code |
02841 |
Country |
South Korea |
|
|
Platform ID |
GPL21507 |
Series (1) |
GSE78230 |
Gene expression-based investigation of a new role for the glyoxylate shunt in contributing to tolerance to oxidative stress. |
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