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Sample GSM261588 Query DataSets for GSM261588
Status Public on Jan 24, 2009
Title 13697374 - sqe1 3 vs ler 3
Sample type RNA
 
Channel 1
Source name ler 3
Organism Arabidopsis thaliana
Characteristics Arabidopsis thaliana (landsberg erecta) - dev.stage (Boyes et al. Plant Cell 2001):boyes: 6.10
Treatment protocol no treatment
Growth protocol leaf - Media=Pots hygrometry=60% RH Temperature=23ºC Light=130 uM/m2seg Long Day
Extracted molecule total RNA
Extraction protocol ler 3:8.17ug.
Label Cy5
Label protocol labeling
 
Channel 2
Source name sqe1 3
Organism Arabidopsis thaliana
Characteristics Arabidopsis thaliana (landsberg erecta) yes - dev.stage (Boyes et al. Plant Cell 2001):boyes: 6.10
Treatment protocol no treatment
Growth protocol leaf - Media=Pots hygrometry=60% RH Temperature=23ºC Light=130 uM/m2seg Long Day
Extracted molecule total RNA
Extraction protocol sqe1 3:9.65ug.
Label Cy3
Label protocol labeling
 
 
Hybridization protocol ler 3 Cy5 / sqe1 3 Cy3 : 30pmol. Hybridization Protocol: CATMA slides (Corning Microarray Technology, CORNING) are pretreated in the prehybridisation solution (1 % BSA, 0.1 SDS, 5X SSC ) at 42°C for 60 min. They are dipped a couple of times in distilled water at room temperature, then in isopropanol and dried immediately by compressed nitrogen stream. Slides were placed in Corning hybridization chambers with a 25x60 lifterslip and 10ul of distilled water for each groove. The target was diluted to a final volume of 60 µL as follows 15µl of purified, labeled cDNA, 15 µl of 4X Hybridization Buffer ( 20X SDS, 0.4 % SDS), 30 µL formamide. The target mixture is heated for 3 min at 95°C, put on ice for 30 sec and centrifuged to remove dust for 1 min. The target mixture was put on the chip as quickly as possible. The microarray is sealed in a chamber and submerged in a 42°C water bath for approximately 16 h. The microarray is washed for 4 min in 1xSSC, 0.2% SDS (42°C); 4 min in 0.1x SSC, 0.2% SDS (RT); 4 min in 0.1x SSC, 0.2% SDS (RT); 4 min in 0.1x SSC (RT); dipped a few times in distilled water and dried immediately by compressed nitrogen stream.
Scan protocol GenePix Pro 3.0, Cy3:pmt voltage 532nm,500V,laser power 35%, Cy5:635nm,pmt voltage 500V,laser power 30%
Description Arabidopsis transcriptome microarray from wild type and mutant plants.
Data processing The raw data comprised the logarithm of median feature pixel intensity at wavelength 635 nm (red) and 532 nm (green). No background was subtracted. An array-by-array normalization was performed to remove systematic biases. First, we excluded spots that were considered badly formed features by the experimenter (Flags=-100). Then we performed a global intensity-dependent normalization using the loess procedure (see Yang et al., 2002) to correct the dye bias. Finally, on each block, the log-ratio median is subtracted from each value of the log-ratio of the block to correct a print-tip effect on each metablock.
 
Submission date Feb 01, 2008
Last update date Feb 05, 2008
Contact name Soubigou-Taconnat Ludivine
E-mail(s) soubigou@evry.inra.fr
Organization name INRA
Department URGV
Lab ADT
Street address 2 rue gaston crémieux
City evry
ZIP/Postal code 91000
Country France
 
Platform ID GPL4346
Series (1)
GSE10349 sqe1-Functional analysis and biotechnological application of genes involved in drought and salt stress tolerance

Data table header descriptions
ID_REF ID number
VALUE Normalized log2 ratio median intensity of Ch2(Cy3)/Ch1(Cy5) (Ch1=reference)

Data table
ID_REF VALUE
1 0.3032
2 1.0045
3 -0.3786
4 -1.6569
5 -1.1533
6 -0.3963
7 -0.9137
8 -0.7061
9 -1.4881
10 -1.8337
11 0.2253
12 -0.7224
13 -0.022
14 0.1102
15 0.0874
16 -0.9551
17 -1.2031
18 -1.0749
19 -0.0062
20 -1.2478

Total number of rows: 25292

Table truncated, full table size 319 Kbytes.




Supplementary file Size Download File type/resource
GSM261588.gpr.gz 2.0 Mb (ftp)(http) GPR
Processed data included within Sample table

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