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Sample GSM555962 Query DataSets for GSM555962
Status Public on Sep 21, 2010
Title early stationary phase_rep 2
Sample type RNA
 
Channel 1
Source name rpoE knockout mutant at early stationary phase of growth
Organism Streptococcus mutans UA159
Characteristics genotype/variation: rpoE knockout
Treatment protocol at normal growth conditons or under different stresses
Growth protocol S. mutans strains were grown in THBY medium at 37°C aerobically (5% CO2 enriched)
Extracted molecule total RNA
Extraction protocol RNA extraction was performed using the RNeasy mini kit (Qiagen).
Label Cy3
Label protocol RNA samples were labelled either with Cy3 or Cy5 using the ULS fluorescent labelling kit (Kreatech, Germany).
 
Channel 2
Source name wild type at early stationary phase of growth
Organism Streptococcus mutans UA159
Characteristics genotype/variation: wildtype
Treatment protocol at normal growth conditons or under different stresses
Growth protocol S. mutans strains were grown in THBY medium at 37°C aerobically (5% CO2 enriched)
Extracted molecule total RNA
Extraction protocol RNA extraction was performed using the RNeasy mini kit (Qiagen).
Label Cy5
Label protocol RNA samples were labelled either with Cy3 or Cy5 using the ULS fluorescent labelling kit (Kreatech, Germany).
 
 
Hybridization protocol 900 ng of each Cy3- and Cy5-labeled RNA was fragmented, and hybridized to the microarray at 65 °C for 17 hours using the Agilent Hybridization Chamber according to the manufacturer’s instructions.
Scan protocol The arrays were scanned using the Agilent DNA Microarray Scanner, and the raw data were extracted using Agilent Feature Extraction software (v9.5).
Description biological replicate 1 of 2, technical replicate 2 of 2, early stationary phase growth, mutant and wild type
Data processing The data were processed by Bioconductor packages written in R language (http://www.r-project.org/). The Linear Models for Microarray analysis (LIMMA) package was used for background correction, Loess-normalization of the two channels of one array, quantile-normalization between different arrays and identification of differentially expressed genes.
 
Submission date Jun 14, 2010
Last update date Sep 21, 2010
Contact name Xiaoli Xue
E-mail(s) [email protected]
Phone +49(0)53161813084
Fax +49(0)53161813096
Organization name Helmholtz Center for Infection Research
Department Cell Biology
Lab Microbial Communication
Street address Inhoffenstr. 7
City Braunschweig
ZIP/Postal code D-38124
Country Germany
 
Platform ID GPL10540
Series (1)
GSE22333 The delta subunit of RNA polymerase, RpoE, is a global modulator of Streptococcus mutans environmental adaptation

Data table header descriptions
ID_REF
VALUE Loess-normalized log2 ratio (Cy3/Cy5)
INV_VALUE Loess-normalized log2 ratio (Cy5/Cy3)

Data table
ID_REF VALUE INV_VALUE
1 -0.27319 0.273189898
2 -0.121572 0.121571792
3 -0.0993255 0.099325528
4 0.0685116 -0.068511602
5 0.460583 -0.460582739
6 -0.149856 0.149856335
7 -0.189638 0.189637925
8 0.116782 -0.116782237
9 -1.40402 1.404015556
10 -0.0580425 0.058042459
11 -0.262185 0.262184694
12 0.384155 -0.384154916
13 -1.99246 1.992460071
14 0.646261 -0.646260833
15 0.0496785 -0.049678512
16 0.527258 -0.527257513
17 0.0562405 -0.056240541
18 1.5933 -1.593298183
19 -0.196911 0.196911235
20 -0.00700771 0.007007714

Total number of rows: 15744

Table truncated, full table size 417 Kbytes.




Supplementary file Size Download File type/resource
GSM555962.txt.gz 4.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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