NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1206650 Query DataSets for GSM1206650
Status Public on Oct 23, 2013
Title WT-ETC-2
Sample type RNA
 
Source name Pseudomonas aeruginosa WT in MOPS pyruvate plus ethylcholine
Organism Pseudomonas aeruginosa
Characteristics genotype: PAO1 wild type
treatment: ethylcholine
Treatment protocol Cell suspension was treated with two volumes of RNA Protect Bacterial Reagent (Qiagen) and processed to a wet pellet as per manufacturer's instructions
Growth protocol Cells were pregrown for 18 h in MOPS with 25 mM pyruvate and 5 mM glucose and then resuspended in MOPS pyruvate or MOPS pyruvate + 250 µM of choline or analogue for four hours
Extracted molecule total RNA
Extraction protocol RNA was extracted from RNA Protect-treated pellets using the Qiagen RNeasy kit using lysozyme-aided lysis. RNA from the first round of columns was treated with DNase I and another round of RNeasy conducted including the on-column DNase step.
Label biotin
Label protocol Biotinylated cDNA was prepared from 50 ng of whole RNA using the NuGen Ovation Pico system and the Encore Biotin Module according to manufacturer's instructions.
 
Hybridization protocol Following fragmentation, 2.4 ug of cRNA were hybridized on the Pseudomonas aeruginosa PAO1 Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix 7G Scanner.
Description WT in pyruvate plus ethylcholine, replicate 2
Data processing Probe intensities were first generated using the AGCC program (Affymetrix). Probe-level intensities were background-corrected, normalized, and summarized, and Robust Multichip Average (RMA) statistics were calculated for each probe set and sample as is implemented in Partek Genomic Suites®, version 6.6
 
Submission date Aug 10, 2013
Last update date Oct 23, 2013
Contact name Matthew J Wargo
E-mail(s) [email protected]
Organization name University of Vermont
Department Department of Microbiology and Molecular Genetics
Street address 95 Carrigan Dr
City Burlington
State/province VT
ZIP/Postal code 05405
Country USA
 
Platform ID GPL84
Series (1)
GSE49759 Characterization of the GbdR regulon in Pseudomonas aeruginosa

Data table header descriptions
ID_REF
VALUE log2 RMA

Data table
ID_REF VALUE
AFFX-YEL002C_WPB1_at 2.154
AFFX-YEL018W_at 2.498
AFFX-YEL024W_RIP1_at 2.177
AFFX-YFL039C_ACT1_at 2.731
AFFX-YER148W_SPT15_at 2.506
AFFX-YER022W_SRB4_at 2.114
AFFX-Athal_GAPDH_at 2.412
AFFX-Athal_ubq_at 2.654
AFFX-Athal_actin_at 2.601
AFFX-Bsubtilis_dapB_at 2.266
AFFX-Bsubtilis_lys_at 2.553
AFFX-Bsubtilis_pheB_at 2.408
AFFX-Bsubtilis_thrC_at 2.747
AFFX-Bsubtilis_trpD_at 2.573
Pae_flgK_at 3.533
Pae_flgL_at 4.509
Pae_orfA_vioA_at 3.501
Pae_orfB_at 3.459
Pae_orfC_at 4.066
Pae_orfD_at 3.796

Total number of rows: 5900

Table truncated, full table size 102 Kbytes.




Supplementary file Size Download File type/resource
GSM1206650_WT-ETC-2.CEL.gz 612.6 Kb (ftp)(http) CEL
Processed data included within Sample table

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