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Sample GSM2069962 Query DataSets for GSM2069962
Status Public on Feb 24, 2016
Title ΔaceA PQ 1mM 2
Sample type RNA
 
Source name PQ 1mM
Organism Pseudomonas aeruginosa PAO1
Characteristics strain: ΔPA2634 transposon insertion mutant
treatment: 1mM PQ
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.
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)
 
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).
Scan protocol The hybridization images were analyzed by GenePix Pro 6.0 (Axon Instruments, CA).
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).
 
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.

Data table header descriptions
ID_REF
VALUE Gene Pix Pro 6.0 (Axon Instruments, CA) was used for background subtraction and GenoWiz 4.0 (Ocimumbiosolutions, India) was used Global normalization.

Data table
ID_REF VALUE
1674714 8.095341793
1674690 9.971336116
1674760 7.594893731
1674678 6.089717327
1674670 7.016547019
1674667 7.356503823
1674687 8.06699721
1674825 5.299170645
1674675 7.295950172
1674681 5.504867472
1674684 7.694604091
1674662 7.80169394
1674720 5.871077087
1674665 4.089717369
1674673 4.714403189
1674699 5.177180155
1674693 4.592429768
1674711 5.972360382
1674702 8.124956179
1674696 9.146815574

Total number of rows: 5545

Table truncated, full table size 102 Kbytes.




Supplementary file Size Download File type/resource
GSM2069962_A_PQ.gpr.gz 1.9 Mb (ftp)(http) GPR
Processed data included within Sample table

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