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Sample GSM231800 Query DataSets for GSM231800
Status Public on Sep 15, 2008
Title Wild-type strain chi7122 exp. 2
Sample type RNA
 
Source Name Wild-type strain chi7122 experiment 2
Organism(s) Escherichia coli
Characteristics E. coli serotype O78:K80:H9, avian pathogenic strain chi7122 grown in LB media [LB broth, per liter, is composed of 10 g of Bacto tryptone, 5 g of yeast extract, 10 g of NaCl and the pH is adjusted to 7.5 by 10 N of NaOH]
Extracted molecule total RNA
Extraction protocol An overnight culture grown at 37°C was diluted 100-fold into 5 ml of LB broth and was allowed to grow to mid-log phase (OD600 0,6). Cultures were centrifuged and RNAs were isolated by using the RiboPure™-Bacteria Kit (Ambion, Austin, TX), according to the manufacturer’s recommendations, with the exception that the DNAse 1 treatment was performed twice.
Label biotin
Label protocol Fragmented cDNA was 3’ biotynylated using GeneChip DNA Labelling Reagent, 7.5 mM (Affymetrix, Santa Clara, CA) and 60 U of Terminal Deoxynucleotidyl Transferase (Promega, Madison, WI) at 37°C for 60 min, as recommended by Affymetrix (www.affymetrix.com). The reaction was stopped by adding 2 µl of 0.5 M EDTA (Sigma) to the reaction mix.
 
Hybridization protocol Hybridization was carried out at McGill University & Genome Quebec Innovation Centre according to Affymetrix recommendation (Affymetrix Expression Manual Section 3 701029 rev. 4).
Scan protocol Scan procedure was carried out at McGill University & Genome Quebec Innovation Centre according to Affymetrix recommendation (Affymetrix Expression Manual Section 3 701029 rev. 4).
Description The cDNA of the chi7122 strain from experience 2 was hybridized onto the GeneChip.
Data processing Data were processed using the FlexArray software (Blazejczyk, M., M. Miron and R. Nadon. 2007. FlexArray: A statistical data analysis software for gene expression microarrays. Genome Quebec, Montreal, Canada. Genome Quebec, Montreal, Canada). Raw data were normalized using the RMA algorithm and log2 were generated. The expression value was generated by subtracting the mean value of each replicate of the mutant strain by wild-type strain.
 
Submission date Sep 26, 2007
Contact name Sébastien Crépin
E-mail(s) sebastien.crepin@umontreal.ca
Organization name Université de Montréal
Department Microbiologie et pathologie
Lab Josée Harel
Street address 3200 Sicotte
City St-Hyacinthe
State/province Québec
ZIP/Postal code J2S7C6
Country Canada
 
Platform ID GPL3154
Series (1)
GSE9178 Genome-wide transcriptional response of an Avian Pathogenic Escherichia coli (APEC) Pst Mutant

Data table header descriptions
ID_REF
VALUE Signal of the probeID after RMA normalization

Data table
ID_REF VALUE
1763843_s_at 6.104147
1761723_at 4.820093
1764051_s_at 6.598927
AFFX-r2-Ec-bioB-M_at 8.454523
1764846_s_at 6.500221
1763201_s_at 8.180779
1761244_s_at 13.21595
1761369_s_at 7.695045
1766228_s_at 7.077927
1766248_at 7.325404
1768106_s_at 3.89608
1767295_at 7.728371
1761489_s_at 5.851784
1761164_s_at 11.12536
1760509_s_at 9.635445
1766665_s_at 7.743835
1767934_at 6.391872
1765262_s_at 10.62364
1768776_s_at 7.908892
1763932_at 11.35183

Total number of rows: 10208

Table truncated, full table size 213 Kbytes.




Supplementary file Size Download File type/resource
GSM231800.CEL.gz 926.8 Kb (ftp)(http) CEL
Raw data provided as supplementary file
Processed data included within Sample table

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