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Sample GSM842265 Query DataSets for GSM842265
Status Public on Sep 18, 2013
Title arcA mutant_CTRL_H2O2_REPLICATE_3
Sample type RNA
 
Channel 1
Source name arcA_mutant_CTRL_REP3
Organism Salmonella enterica subsp. enterica serovar Typhimurium str. 14028S
Characteristics genotype/variation: arcA mutant
stress: CTRL
Extracted molecule total RNA
Extraction protocol High Pure RNA isolation kit (Roche)
Label Cy5
Label protocol Incorporation of dye using about 1200U Superscript II reverse transcriptase (Invitrogen, Carlsbad, CA), 40ng/ul random hexamer primers, 4nmol Cy dUTP (GE Healthcare, Fairfield, CT), and 80U RNAse Inhibitor (Roche, Indianapolis, IN), in 60ul reactions. Reverse transcription was performed for 2h at 42˚C, and the pH adjusted with 50mM NaOH. After a 10min incubation at 70˚C reactions were neutralized using HCl. Labeled cDNA was purified using the QIAGEN PCR purification kit as suggested by the manufacturer (Qiagen, Valencia, CA).
 
Channel 2
Source name arcA_mutant_H2O2_REP3
Organism Salmonella enterica subsp. enterica serovar Typhimurium str. 14028S
Characteristics genotype/variation: arcA mutant
stress: H2O2
growth protocol: arcA minus salmonella grown to OD600 0.4 in 25 ml LB medium, and treated with 1.5 mM H2O2 for 20 min. replicate 03
Extracted molecule total RNA
Extraction protocol High Pure RNA isolation kit (Roche)
Label Cy3
Label protocol Incorporation of dye using about 1200U Superscript II reverse transcriptase (Invitrogen, Carlsbad, CA), 40ng/ul random hexamer primers, 4nmol Cy dUTP (GE Healthcare, Fairfield, CT), and 80U RNAse Inhibitor (Roche, Indianapolis, IN), in 60ul reactions. Reverse transcription was performed for 2h at 42˚C, and the pH adjusted with 50mM NaOH. After a 10min incubation at 70˚C reactions were neutralized using HCl. Labeled cDNA was purified using the QIAGEN PCR purification kit as suggested by the manufacturer (Qiagen, Valencia, CA).
 
 
Hybridization protocol 42C overnight in standard hybridization buffer (Roche Nimblegen)
Scan protocol GenePix4000B scanner (Molecular Devices, Sunnyvale, CA) using Acuity 4.0 software.
Description EM_420460_AP3_Cy3_ch2_AC3_Cy5_ch1
Data processing Signal extraction and quantitation with Roche’s NimbleScan 2.4 package
log base 10 ratios of contributions to total signal (experimental condition / control)
normalized based on total signal for each channel
 
Submission date Dec 04, 2011
Last update date Sep 18, 2013
Contact name Michael McClelland
E-mail(s) mcclelland.michael@gmail.com
Phone 858-336-9554
Organization name University of California, Irvine
Department Microbiology & Molecular Genetics
Street address 132 Med Surge I
City Irvine
State/province CA
ZIP/Postal code 92697
Country USA
 
Platform ID GPL14855
Series (1)
GSE34134 Role of the ArcAB two-component system in oxidative stress

Data table header descriptions
ID_REF
VALUE log base 10 ratios of contributions to total signal (experimental condition / control)

Data table
ID_REF VALUE
MMCCSAL07_00001 0.220220139
MMCCSAL07_00002 0.657850481
MMCCSAL07_00003 0.435427527
MMCCSAL07_00004 0.757404363
MMCCSAL07_00005 0.634716237
MMCCSAL07_00006 0.577424415
MMCCSAL07_00007 0.405986169
MMCCSAL07_00008 0.733157693
MMCCSAL07_00009 0.677423755
MMCCSAL07_00010 0.537340153
MMCCSAL07_00011 0.770036636
MMCCSAL07_00012 0.525301321
MMCCSAL07_00013 0.726166488
MMCCSAL07_00014 0.597739363
MMCCSAL07_00015 0.608344581
MMCCSAL07_00016 0.535432446
MMCCSAL07_00017 0.772977337
MMCCSAL07_00018 0.710848582
MMCCSAL07_00019 0.489491647
MMCCSAL07_00020 0.591351924

Total number of rows: 392936

Table truncated, full table size 11042 Kbytes.




Supplementary file Size Download File type/resource
GSM842265.txt.gz 5.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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