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Sample GSM545493 Query DataSets for GSM545493
Status Public on Nov 19, 2010
Title water treated plant vs BABA treated plant replicate 1
Sample type RNA
 
Channel 1
Source name rosette leaves from BABA treated plants
Organism Arabidopsis thaliana
Characteristics ecotype: Col-0
treatment: BABA
Extracted molecule total RNA
Extraction protocol Total RNA extracted using lithium chloride 6M overnight at 4C
Label Cy5
Label protocol Total RNA from leaves was amplified using the MessageAmpTM aRNA II kit (Ambion, NY, U.S.A.). 5 microgram of amplified RNA were reverse transcribed into cyanin3 or cyanin 5 labeled cDNA, purified with QiaquickTM columns (Qiagen, Netherlands) and hybridized on custom microarrays (GEO accession number GPL6147)
 
Channel 2
Source name rosette leaves from water treated plants
Organism Arabidopsis thaliana
Characteristics ecotype: Col-0
treatment: H2O
Extracted molecule total RNA
Extraction protocol Total RNA extracted using lithium chloride 6M overnight at 4C
Label Cy3
Label protocol Total RNA from leaves was amplified using the MessageAmpTM aRNA II kit (Ambion, NY, U.S.A.). 5 microgram of amplified RNA were reverse transcribed into cyanin3 or cyanin 5 labeled cDNA, purified with QiaquickTM columns (Qiagen, Netherlands) and hybridized on custom microarrays (GEO accession number GPL6147)
 
 
Hybridization protocol Hybridisation buffer was 3xSSC and 0,4%SDS. Incubation at 64°C O/N without agitation. Washing conditions: twice for 5 minutes in 2xSSC 0.1% SDS, twice for 1 minute in 0.2xSSC, 1 minute in 0.1xSSC, 5 minutes in 0.1xSSC 0.1% TritonX100. All washes at room temperature.
Scan protocol Agilent microarray scanner, 10 μm resolution
Description water_BABA1
CA 790
Data processing GenePix Pro 6.0 was used to analyse the images and generate gpr files; raw data without background substraction were print-tip loess normalized to calculate M values. LimmaGui software package (Wettenhall, J. M., and Smyth, G. K. (2004). limmaGUI: a graphical user interface for linear modeling of microarray data. Bioinformatics, 20:3705-3706) was used for data analysis.
 
Submission date May 20, 2010
Last update date Nov 19, 2010
Contact name Johann Weber
Organization name University of Lausanne
Department Center for integrative Genomics
Lab DNA array facility
Street address Genopode Building
City Lausanne
State/province VD
ZIP/Postal code CH 1015
Country Switzerland
 
Platform ID GPL6147
Series (1)
GSE16434 Analysis of gene expression in Arabidopsis thaliana after priming with BABA and infection with Pseudomonas syringae pv tomato DC3000

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

Data table
ID_REF VALUE
CATMA1a00010 0.254021656
CATMA1a00020 0.073735853
CATMA1a00030 -0.113391833
CATMA1a00035 0.654625114
CATMA1a00040 -0.285287977
CATMA1a00045 -0.293642796
CATMA1a00050 -0.191057638
CATMA1a00060 0.037972572
CATMA1a00070 -0.092802928
CATMA1a00080 -0.183279097
CATMA1a00090 -0.015319062
CATMA1a00090_bis -0.000847728
CATMA1a00100 0.117975746
CATMA1a00110 0.023211358
CATMA1a00130 0.148047834
CATMA1a00140 0.16343443
CATMA1a00150 0.062419816
CATMA1a00160 0.222533687
CATMA1a00170 -0.119647104
CATMA1a00180 -0.325116622

Total number of rows: 24966

Table truncated, full table size 619 Kbytes.




Supplementary file Size Download File type/resource
GSM545493.gpr.gz 1.9 Mb (ftp)(http) GPR
Processed data included within Sample table

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