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Sample GSM870034 Query DataSets for GSM870034
Status Public on Jan 31, 2013
Title WTvsKOhdiR CDML replicate 1
Sample type RNA
 
Channel 1
Source name LMD-9WT CDML OD 0.4
Organism Streptococcus thermophilus
Characteristics strain: LMD-9
isolate: clone 1
Growth protocol Strains LMD-9 WT and CB0082 were grown at 37°C during 16h in M17 medium supplemented with lactose 1% (M17L), washed twice (5,000 x g, 9 min, room temperature) in one volume of CDM medium supplemented with lactose 1% (CDML) and resuspended in one volume of CDML. Cultures were then 30-fold diluted in CDML. When cells reached the mid-log phase (OD600 of 0.4), 25-ml aliquots were collected for total RNA extraction.
Extracted molecule total RNA
Extraction protocol Cells were harvested by centrifugation (7,000 x g for 4 min) and mechanically broken with 0.18-mm-diameter glass beads in a Braun Homogenizer (three 1-min periods of homogenization with 1-min intervals on ice). Total RNA was extracted using the High Pure RNA isolation kit (ROCHE, Basel, Switzerland)
Label Alexa Fluor 555
Label protocol First strand cDNA was synthetized from 10 microg RNA. Synthesized cDNA were purified and labeled with Alexa Fluor 555 and Alexa Fluor 647. Experiments were carried out according to instructions of the Superscript Plus Indirect cDNA Labeling system (Invitrogen).
The quality of the labeled cDNA and its concentration were respectively measured with the 2100 Bioanalyser (Agilent Technologies, Santa Clara, CA) and ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE).
 
Channel 2
Source name KOhdiR CDML OD 0.4
Organism Streptococcus thermophilus
Characteristics isolate: clone 1
strain: CB0082
Growth protocol Strains LMD-9 WT and CB0082 were grown at 37°C during 16h in M17 medium supplemented with lactose 1% (M17L), washed twice (5,000 x g, 9 min, room temperature) in one volume of CDM medium supplemented with lactose 1% (CDML) and resuspended in one volume of CDML. Cultures were then 30-fold diluted in CDML. When cells reached the mid-log phase (OD600 of 0.4), 25-ml aliquots were collected for total RNA extraction.
Extracted molecule total RNA
Extraction protocol Cells were harvested by centrifugation (7,000 x g for 4 min) and mechanically broken with 0.18-mm-diameter glass beads in a Braun Homogenizer (three 1-min periods of homogenization with 1-min intervals on ice). Total RNA was extracted using the High Pure RNA isolation kit (ROCHE, Basel, Switzerland)
Label Alexa Fluor 647
Label protocol First strand cDNA was synthetized from 10 microg RNA. Synthesized cDNA were purified and labeled with Alexa Fluor 555 and Alexa Fluor 647. Experiments were carried out according to instructions of the Superscript Plus Indirect cDNA Labeling system (Invitrogen).
The quality of the labeled cDNA and its concentration were respectively measured with the 2100 Bioanalyser (Agilent Technologies, Santa Clara, CA) and ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE).
 
 
Hybridization protocol Hybridization of the labeled cDNA (0.3 microg per sample) were added to hybridization buffer (Agilent In Situ Hybridization Kit Plus) and samples were applied to microarrays enclosed in Agilent SureHyb-enabled hybridization chambers. After hybridization, slides were washed sequentially according to Agilent instructions.
Scan protocol Scanned on an Agilent Scanner G2565B
Images were quantified using Agilent Feature Extraction Software (version 9.1).
Description Biological replicate 1 of 2
Data processing Agilent Feature Extraction Software (v 9.1) was used for background subtraction and LOWESS normalization.
 
Submission date Feb 02, 2012
Last update date Jan 31, 2013
Contact name Pascal Hols
E-mail(s) pascal.hols@uclouvain.be
Phone +32 10 47 88 96
Fax +32 10 47 31 09
Organization name Université catholique de louvain
Department Institut des Sciences de la Vie
Lab Biochimie et Génétique Moléculaire Bactérienne
Street address Place Croix du Sud 5
City Louvain-La-Neuve
ZIP/Postal code 1348
Country Belgium
 
Platform ID GPL13365
Series (1)
GSE35517 WT vs KO hdiR comparison

Data table header descriptions
ID_REF
VALUE normalized log10 ratio Cy5/Cy3

Data table
ID_REF VALUE
1 2.827346674e-001
2 0.000000000e+000
3 0.000000000e+000
4 -1.534261905e-003
5 -1.075550569e-001
6 -3.157818863e-002
7 -7.017380339e-002
8 8.076186742e-002
9 -5.446991623e-002
10 -6.369665017e-002
11 -1.139528919e-002
12 1.149408498e-002
13 8.584479391e-002
14 2.044741996e-001
15 -6.708108047e-002
16 6.359631142e-003
17 4.686448557e-002
18 -6.658636082e-003
19 5.929709186e-002
20 2.872822705e-002

Total number of rows: 15744

Table truncated, full table size 350 Kbytes.




Supplementary file Size Download File type/resource
GSM870034_US45102921_252334210002_S01_GE2-v5_91_0806_2_1.txt.gz 4.5 Mb (ftp)(http) TXT
Processed data included within Sample table

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