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Sample GSM3015447 Query DataSets for GSM3015447
Status Public on Apr 11, 2018
Title E.coli_Na20_rep1
Sample type RNA
 
Source name Escherichia coli CC72 NaCl 20 min
Organism Escherichia coli str. K-12 substr. MG1655
Characteristics substrain: CC72
genotype: Fusion of venus to the 3' end of rpoC in E. coli wild-type MG1655
Treatment protocol When the OD600 of the cell culture reached 0.2, solid NaCl was added and dissolved to a final concentration of 0.5 M to induce osmotic stress. After 0.5 M NaCl treatment for 10 min, 20 min and 45 min, samples were collected, respectively.
Growth protocol E. coli CC72 was grown in water bath to early-exponential phase (OD600 0.2) at 37°C in LB medium, then samples were collected.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the RNeasy Mini kit (Qiagen Inc., Valencia, CA, USA) and the RNAprotect reagent (Qiagen) and DNA was removed by on-column DNase digestion with the RNase-Free DNase set (Qiagen). RNA quality and concentration was determined by analysis with an Agilent 2100 bioanalyzer.
Label Cy3
Label protocol Labeling was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
 
Hybridization protocol Hybridization was performed by NimbleGen Systems Inc., Madison, WI, USA following their standard operating protocol. See www.nimblegen.com.
Scan protocol Scanning was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
Description NC_000913.2+NC_000913.3
This sample is E. coli CC72 grown in LB medium after 0.5 M NaCl shock for 20 min. It is the first of two biological replicates used in this experiment, each from separate cultures.
Data processing Expression values were generated using quantile normalization (Bolstad et al., 2003, Bioinformatics, 19:185), and the Robust Multichip Average (RMA) algorithm (Irizarry et al., 2003, Nucleic Acids Res. 31: e15 and Irizarry et al., 2003, Biostatistics 4:249) based on the raw data (.pair file) and background correction as implemented in the NimbleScan software package (Roche NimbleGen, Inc.).
 
Submission date Feb 16, 2018
Last update date Apr 12, 2018
Contact name Zhe Sun
Organization name Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences
Street address 32 West 7th Ave
City Tianjin
ZIP/Postal code 300308
Country China
 
Platform ID GPL14649
Series (1)
GSE110730 Expression analysis of Escherichia coli CC72 before and after osmotic stress

Data table header descriptions
ID_REF
VALUE RMA-normalized, averaged gene-level signal intensity

Data table
ID_REF VALUE
b0001071000000001 935.902
b0002071000000002 10808.91295
b0003071000000003 4407.6908
b0004071000000004 567.6654
b0005071000000005 319.72915
b0006071000000006 98.8863
b0007071000000007 965.384
b0008071000000008 3087.1724
b0009071000000009 270.1881
b0010071000000010 305.5441
b0011071000000011 105.62935
b0013071000000012 77.40935
b0014071000000013 34114.06415
b0015071000000014 5580.193
b0016071000000015 1997.28025
b0018071000000016 100.0042
b0019071000000018 8681.96695
b0020071000000019 890.8197
b0021071000000020 4531.09255
b0022071000000021 5980.34225

Total number of rows: 4254

Table truncated, full table size 114 Kbytes.




Supplementary file Size Download File type/resource
GSM3015447_Na20-1N.pair.gz 1.0 Mb (ftp)(http) PAIR
GSM3015447_Na20-1R.pair.gz 1011.6 Kb (ftp)(http) PAIR
Processed data included within Sample table
Processed data provided as supplementary file

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