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Status |
Public on Nov 19, 2010 |
Title |
water treated plant vs BABA treated plant replicate 1 |
Sample type |
RNA |
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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)
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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)
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|
|
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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.
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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 |
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|
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 |
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