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Sample GSM1608468 Query DataSets for GSM1608468
Status Public on Jul 28, 2015
Title ST WT biol1 over ST rpoN_compl biol1
Sample type RNA
 
Channel 1
Source name WT cells grown statically until OD(600nm)=0.2
Organism Bacillus cereus ATCC 14579
Characteristics strain derivative: WT
Treatment protocol Cells were harvested at above mentioned timepoints (see overall design) without any additional treatment.
Growth protocol Liquid cultures of B. cereus ATCC14579 WT, ΔrpoN and ΔrpoN-comp strains were grown in BHI with aeration (200rpm) and statically in Erlenmeyer flasks at 30°C.
Extracted molecule total RNA
Extraction protocol Cultures were spinned down, resuspended in 1 ml TRI reagent (Ambion) and snap frozen in liquid nitrogen. RNA was extracted according to the RNAwiz (Ambion) protocol using Chloroform/isopropanol extraction. Residual DNA was enzymatically removed using the TURBO DNA-free (Ambion) kit following the instructions of the manufacturer.
Label cy3
Label protocol Cy3 and Cy5 labeling of the cDNA was performed with CyScribe Post-Labeling kit (GE Healthcare)
 
Channel 2
Source name rpoN-comp complemented mutant cells grown statically until OD(600nm)=0.2
Organism Bacillus cereus ATCC 14579
Characteristics strain derivative: ΔrpoN-comp
Treatment protocol Cells were harvested at above mentioned timepoints (see overall design) without any additional treatment.
Growth protocol Liquid cultures of B. cereus ATCC14579 WT, ΔrpoN and ΔrpoN-comp strains were grown in BHI with aeration (200rpm) and statically in Erlenmeyer flasks at 30°C.
Extracted molecule total RNA
Extraction protocol Cultures were spinned down, resuspended in 1 ml TRI reagent (Ambion) and snap frozen in liquid nitrogen. RNA was extracted according to the RNAwiz (Ambion) protocol using Chloroform/isopropanol extraction. Residual DNA was enzymatically removed using the TURBO DNA-free (Ambion) kit following the instructions of the manufacturer.
Label cy5
Label protocol Cy3 and Cy5 labeling of the cDNA was performed with CyScribe Post-Labeling kit (GE Healthcare)
 
 
Hybridization protocol Hybridization was performed as described in Mols et al., 2013.
Scan protocol Slides were scanned with Agilent G2505C scanner
Description Expression profiles of the rpoN deletion mutant (ΔrpoN) and the complemented strain (ΔrpoN-comp) were compared to the parental strain (WT) at static growth
Data processing Data were normalized using Lowess normalisation as available in MicroPrep and corrected for inter-slide differences. Median intensity of the different probes per gene and biological replicate was selected as the gene expression intensity.
 
Submission date Feb 12, 2015
Last update date Jul 28, 2015
Contact name Jos Boekhorst
E-mail(s) Jos.Boekhorst@nizo.com
Organization name NIZO food research
Street address Kernhemseweg 2
City Ede
ZIP/Postal code 6718 ZB
Country Netherlands
 
Platform ID GPL19768
Series (1)
GSE65894 Transcriptome comparison between Bacillus cereus ATCC 14579 wildtype (WT), RpoN (Sigma 54) deletion mutant and the complemented strain.

Data table header descriptions
ID_REF
VALUE log2 of normalized ratio (Cy5/Cy3)
PRE_VALUE Normalized ratio (Cy5/Cy3)

Data table
ID_REF VALUE PRE_VALUE
BC0001 0.5889 1.504142587
BC0002 0.4406 1.357181307
BC0003 0.3719 1.294091474
BC0004 0.2101 1.156737987
BC0005 0.3414 1.266950027
BC0006 0.1147 1.082761033
BC0012 0.2115 1.157855391
BC0013 -1.7266 0.302164219
BC0014 -0.1582 0.896156454
BC0015 0.0737 1.052448144
BC0016 0.0400 1.02808335
BC0017 0.4279 1.34524788
BC0019 0.8885 1.851312009
BC0020 1.2079 2.310068028
BC0021 1.0148 2.020616516
BC0022 -0.0938 0.937044178
BC0023 0.5823 1.497246958
BC0024 0.7282 1.656576263
BC0025 -0.2899 0.817950977
BC0026 0.3429 1.268288192

Total number of rows: 5270

Table truncated, full table size 134 Kbytes.




Supplementary file Size Download File type/resource
GSM1608468_US22502548_251734310075_S01_GE2_107_Sep09_1_4.txt.gz 3.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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