NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1341347 Query DataSets for GSM1341347
Status Public on Sep 11, 2014
Title WT_CPR_2
Sample type RNA
 
Source name Cirpofloxacin treated WT sample at T1h, biological rep 2
Organism Escherichia coli K-12
Characteristics background strain: BW25113
genotype/variation: wild type
Treatment protocol We compared the microarray-determined mRNA profiles (Affymetrix E. coli Genome 2.0 Array) of Δfur and WT genotypes in response to ciprofloxacin treatment (100 ng/ml) with those of untreated cultures. We used two biological replicates per genotype.
Growth protocol Escherichia coli BW25113 and fur mutant strains were cultivated at 37Co in 25 ml of LB medium using Erlenmeyer flasks. 1 ml of OVN culture was transferred to 20 ml of fresh LB medium and cells were incubated in the presence or absence of ciprofloxacin (100 ng/ml).
Extracted molecule total RNA
Extraction protocol Samples for microarray analyses were taken before ciprofloxacin treatment (t0) and then at 1 hour post-treatment (t1). Cell concentration was adjusted to 109 cells/ml and cultures were treated with ciprofloxacin in Erlenmeyer flasks using 20 ml fresh LB. ~109 cells were taken at each timepoint as samples for RNA isolation. In order to stabilize RNA, RNA Bacteria Protect Reagent (Qiagen) was added to the samples according to the instructions of the manufacturer and then samples were stored overnight at -80°C. Total RNA was isolated by using RNeasy Mini Kit (Qiagen) according to the manufacturer’s instructions. Sample concentration was estimated using the NanoDrop 1000 (Thermoscientific) spectrophotometer.
Label biotin
Label protocol Biotinylated cDNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Hybridization of the cDNAs was conducted at UD-GenoMed Medical Genomic Technologies Ltd. (4032, Debrecen, Nagyerdei Krt. 98. Tel: +36 30 494 6496) using Affymetrix Genechip® E. coli Genome 2.0 Array (Affymetrix) as described by the manufacturer.
Scan protocol Arrays were scanned on GeneChip Scanner 7G (Affymetrix), Affymetrix GeneChip Command Console (AGCC) was used to obtain image files (DAT/CEL).
Description Escherichia coli liquid culture, incubated in LB medium, BW25113
Data processing CHP files were generated using Affymetrix Expression Control. Downstream data analysis was performed in GeneSpring GX 12, CEL files were imported using RMA algorithm and median normalization was performed.
 
Submission date Mar 06, 2014
Last update date Sep 11, 2014
Contact name Balazs Bogos
E-mail(s) bogos.balazs@mta.brc.hu
Phone +36-62-599-693
Organization name Biological Research Centre of the Hungarian Academy of Sciences
Department Institute of Biochemistry
Lab Laboratory of Microbial Experimental Evolution
Street address Temesvári krt. 62-64
City Szeged
ZIP/Postal code 6724
Country Hungary
 
Platform ID GPL3154
Series (1)
GSE55662 Plasticity of transcriptional regulation under antibiotic stress

Data table header descriptions
ID_REF
VALUE log2-RMA signal

Data table
ID_REF VALUE
AFFX-BioB-5_at 10.54
AFFX-BioB-M_at 10.78
AFFX-BioB-3_at 10.75
AFFX-BioC-5_at 9.84
AFFX-BioC-3_at 9.27
AFFX-BioDn-5_at 9.57
AFFX-BioDn-3_at 10.05
AFFX-CreX-5_at 4.07
AFFX-CreX-3_at 5.44
AFFX-DapX-5_at 12.24
AFFX-DapX-M_at 12.23
AFFX-DapX-3_at 12.16
AFFX-LysX-5_at 10.86
AFFX-LysX-M_at 10.57
AFFX-LysX-3_at 10.49
AFFX-PheX-5_at 11.33
AFFX-PheX-M_at 11.16
AFFX-PheX-3_at 10.92
AFFX-ThrX-5_at 11.7
AFFX-ThrX-M_at 11.44

Total number of rows: 10208

Table truncated, full table size 177 Kbytes.




Supplementary file Size Download File type/resource
GSM1341347_04_E_coli_2_.CEL.gz 840.8 Kb (ftp)(http) CEL
GSM1341347_04_E_coli_2_.rma.chp.gz 85.6 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap