NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM307117 Query DataSets for GSM307117
Status Public on Nov 01, 2008
Title Planktonic cells stat phase, biological replicate 3
Sample type RNA
 
Source name P. aeruginosa planktonic cells after 9h of growth
Organism Pseudomonas aeruginosa
Characteristics Cultures pigmented, OD~9
Treatment protocol All cells were harvested directly into RNAlater (Ambion), kept at 5degC overnight and stored at -80degC until use.
Growth protocol All samples were grown in AGSY medium (56 mM alanine, 17 mM K2HPO4, 86 mM NaCl, 100 μM CaCl2, 10 mM MgSO4, 5 µM FeCl2, 7.5 µM ZnCl2, 0.5% v/v glycerol, 3 g/L yeast extract, pH 7) at 37degC. Planktonic cells were grown with vigorous shaking for three hours (late exponential phase) or nine hours (early stationary phase), colonies were grown on 1.5% agar for 15 or 40 hours, and biofilms were grown for three days in silicone tubes, 6 mm i.d. under a continuous flow of 50 ml/h for 3 days.
Extracted molecule total RNA
Extraction protocol RNA was extracted using the RNeasy Mini Purification Kit (Qiagen) following the supplier's instructions.
Label biotin
Label protocol Biotinylated RNA was prepared from 12 mg total RNA as previously described (Hentzer et al. 2005, Biofilms 2, 27-61).
 
Hybridization protocol Following fragmentation, cDNA was hybridized for 16 hr at 50degC on GeneChip P. aeruginosa Genome Arrays. The GeneChips were then washed and stained in an Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using a GeneChip Scanner 3000 (Affymetrix).
Description Genee expresion data from planktonic cells in early stationary phase
Data processing Preliminary data processing was performed using Affymetrix GCOS 1.4 and total signal target was scaled to 500 for all arrays. Normalisation was performed using
The resulting output data was analysed using R 2.5.0 (r-project.org) and the BioConductor packages affyPLM, GCRMA and LIMMA (bioconductor.org).
Normalisation was carried out using quantile normalisation, no background correction, perfect match probes only and median polish summary.
 
Submission date Jul 22, 2008
Last update date Sep 30, 2008
Contact name Helga Mikkelsen
E-mail(s) h.mikkelsen@imperial.ac.uk
Phone 01223 333 640
Organization name University of Cambridge
Department Department of Biochemistry
Lab M. Welch lab
Street address Building O, Downing Site
City Cambridge
ZIP/Postal code CB2 1HA
Country United Kingdom
 
Platform ID GPL84
Series (1)
GSE12207 Biofilms and type III secretion are not mutually exclusive in Pseudomonas aeruginosa

Data table header descriptions
ID_REF
VALUE Signal intensity.

Data table
ID_REF VALUE
AFFX-Athal_actin_at 8.37174484798799
AFFX-Athal_GAPDH_at 8.23368759490682
AFFX-Athal_ubq_at 8.53662585803922
AFFX-Bsubtilis_dapB_at 8.67936053128625
AFFX-Bsubtilis_lys_at 8.29997495922716
AFFX-Bsubtilis_pheB_at 8.47705035515156
AFFX-Bsubtilis_thrC_at 8.62070168785265
AFFX-Bsubtilis_trpD_at 8.35007857612388
AFFX-YEL002C_WPB1_at 8.13558298939275
AFFX-YEL018W_at 8.3173347532176
AFFX-YEL024W_RIP1_at 8.33240429128056
AFFX-YER022W_SRB4_at 8.15402938294077
AFFX-YER148W_SPT15_at 8.3609636431185
AFFX-YFL039C_ACT1_at 8.39923498968354
ig_1046911_1047549_at 8.98492697929841
ig_1047549_1046911_at 8.5428440031704
ig_1063544_1064555_at 8.84725116200736
ig_1064555_1063544_at 8.78421095592069
ig_1087095_1087843_at 9.06746753402496
ig_1087843_1087095_at 9.15680781189898

Total number of rows: 5900

Table truncated, full table size 165 Kbytes.




Supplementary file Size Download File type/resource
GSM307117.CEL.gz 764.7 Kb (ftp)(http) CEL
Processed data included within Sample table

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