NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM954580 Query DataSets for GSM954580
Status Public on Oct 15, 2012
Title PW5126-1
Sample type RNA
 
Source name Cells harvested at OD 600 nm of 0.5
Organism Pseudomonas aeruginosa
Characteristics strain: PW5126
genotype: PA2449-E03::ISphoA/hah
Treatment protocol At an OD 600 nm of 0.5, 0.5 mL of culture was treated with 1.0 mL of RNAprotect Bacterial reagent (Qiagen).
Growth protocol P. aeruginosa PAO1-UW or PW5126 was grown in 50-mL of peptone broth (per liter: 20 grams peptone derived from gelatin, 10 g K2SO4, and 1.5 MgSO4) at 37 C, 200 rpm, until an OD 600 of 0.5 was reached.
Extracted molecule total RNA
Extraction protocol RNA was isolated using the enzymatic lysis and proteinase K digestion method of Qiagen Rneasy with on-column DNA digestion.
Label biotin
Label protocol Samples were processed according to the Prokaryotic Target Preparation Protocol in Affymetrix GeneChip Expression Analysis Technical Manual. Briefly, 10 ug of RNA was used to synthesize cDNA via random primers and SuperScript II reverse transcriptase. cDNA was purified using Qiagen MinElute PCR purification columns. The resulting cDNA was fragmented and labeled with biotin.
 
Hybridization protocol Following fragmentation, 5 ug of cDNA were hybridized for 16 hr at 50C 60 rpm on GeneChip P. aeruginosa Genome Array with rotation at 60 rpm. GeneChips were processed with an Affymetrix Fluidics Station 450 using the modified Flex FS450_0002 P. aeruginosa array protocol (as specified in the Affymetrix GeneChip Expression Analysis Technical Manual), using stains from the Affymetrix Hybridization, Wash, and Stain Kit.
Scan protocol Arrays were scanned with the Affymetrix GeneChip Scanner 7G Plus
Description Gene expression from mid-exponential cells grown in rich media
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method.
 
Submission date Jul 02, 2012
Last update date Oct 15, 2012
Contact name Christopher Nomura
E-mail(s) [email protected]
Phone 315-470-6854
Organization name SUNY-ESF
Department Chemistry
Lab 336 Jahn
Street address 1 Forestry Dr.
City Syracuse
State/province NY
ZIP/Postal code 13210
Country USA
 
Platform ID GPL84
Series (1)
GSE39044 Regulon of transcriptional regulator PA2449 in Pseduomonas aeruginosa PAO1

Data table header descriptions
ID_REF
VALUE MAS5.0 signal intensity
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-YEL002C_WPB1_at 0.3 A 0.964837
AFFX-YEL018W_at 0.7 A 0.968686
AFFX-YEL024W_RIP1_at 8.6 A 0.150527
AFFX-YFL039C_ACT1_at 20.2 A 0.250724
AFFX-YER148W_SPT15_at 7 A 0.892699
AFFX-YER022W_SRB4_at 1.3 A 0.951005
AFFX-Athal_GAPDH_at 0.5 A 0.765443
AFFX-Athal_ubq_at 31.9 A 0.267463
AFFX-Athal_actin_at 0.7 A 0.837065
AFFX-Bsubtilis_dapB_at 24670.7 P 0.000219
AFFX-Bsubtilis_lys_at 847 P 0.000468
AFFX-Bsubtilis_pheB_at 9885.5 P 0.000219
AFFX-Bsubtilis_thrC_at 9063.2 P 0.000219
AFFX-Bsubtilis_trpD_at 1.7 A 0.956032
Pae_flgK_at 16.5 A 0.513937
Pae_flgL_at 4.8 A 0.992047
Pae_orfA_vioA_at 70.7 A 0.253373
Pae_orfB_at 83.6 A 0.231536
Pae_orfC_at 65.1 A 0.458256
Pae_orfD_at 13 A 0.9768

Total number of rows: 5900

Table truncated, full table size 164 Kbytes.




Supplementary file Size Download File type/resource
GSM954580_Nomura_PA2449-1_Pae_G1a_.CEL.gz 602.4 Kb (ftp)(http) CEL
Processed data included within Sample table

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