NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM986575 Query DataSets for GSM986575
Status Public on Aug 01, 2017
Title tomato leaves at 12 hpt with water, biological rep1
Sample type RNA
 
Source name leaves at 12 hpt with water
Organism Solanum lycopersicum
Characteristics cultivar: Summer sweet
treatment: water
time (post-treatment): 12 hours
tissue: leaves
Treatment protocol Tomato plants were sprayed thoroughly with NPA or water until run-off. For preparation of NPA, 1 g phosphorous acid (Sigma-Aldrich, St. Louis, MO, USA) was mixed with 1 L ddH2O, followed by the addition of 1 g potassium hydroxide (Sigma-Aldrich) to adjust the pH to 6.3.
Growth protocol Seedlings of tomato were grown on a mixture of peat moss, perlite and vermiculite at 27oC under a 12 hour photoperiod.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNAs were prepared with 10 μg of plant total RNA according to the standard Affymetrix protocol (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 μg of cRNA were hybridized with GeneChip Tomato Genome Array at 45oC for 16 hours. Subsequently, GeneChips were washed and stained in the Affymetrix GeneChip fluidics station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip scanner 3000.
Description Gene expression data from tomato leaves 12 hours after water treatment
Data processing The raw data were analyzed by using Gene-Spring® GX 10 (Agilent Technologies) based on the Robust Multi-array Average (RMA) algorithm. The processes included background correction, log2 transformation, quantile normalization, and conversion to obtain an expression measure for each probe set on each array. As referring to the histogram of the expression value, normalized probe signal values less than 5.5 in all of the chips were considered to be the result of nonspecific hybridization, and then resulted in 8488 probes.
 
Submission date Aug 16, 2012
Last update date Aug 01, 2017
Contact name Ruey-Fen Liou
E-mail(s) rfliou@ntu.edu.tw
Organization name National Taiwan University
Department Plant Pathology and Microbiology
Street address 1, Sec. 4, Roosevelt Road
City Taipei
ZIP/Postal code 106
Country Taiwan
 
Platform ID GPL4741
Series (2)
GSE40163 Transcriptome analysis of tomato in response to treatment with neutralized phosphorous acid (NPA)
GSE40214 Transcriptome analysis of neutralized phosphorous acid (NPA)-induced resistance in tomato against Phytophthora parasitica

Data table header descriptions
ID_REF
VALUE Log2 RMA signal

Data table
ID_REF VALUE
AFFX-BioB-5_at 8.45
AFFX-BioB-M_at 8.20
AFFX-BioB-3_at 8.03
AFFX-BioC-5_at 9.50
AFFX-BioC-3_at 9.84
AFFX-BioDn-5_at 10.98
AFFX-BioDn-3_at 11.77
AFFX-CreX-5_at 13.47
AFFX-CreX-3_at 13.86
AFFX-DapX-5_at 9.36
AFFX-DapX-M_at 10.37
AFFX-DapX-3_at 10.23
AFFX-LysX-5_at 6.30
AFFX-LysX-M_at 6.37
AFFX-LysX-3_at 7.74
AFFX-PheX-5_at 6.86
AFFX-PheX-M_at 7.08
AFFX-PheX-3_at 7.37
AFFX-ThrX-5_at 7.36
AFFX-ThrX-M_at 7.97

Total number of rows: 8488

Table truncated, full table size 200 Kbytes.




Supplementary file Size Download File type/resource
GSM986575_CK_12hpt_1.CEL.gz 951.5 Kb (ftp)(http) CEL
Processed data included within Sample table

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