NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM5568968 Query DataSets for GSM5568968
Status Public on Sep 27, 2021
Title flg15-sprayed, experiment 2, biological rep2
Sample type RNA
 
Source name Leaves of Solanum lycopersicum 24 hours after spray treatment
Organism Solanum lycopersicum
Characteristics tissue: leaves
treatment: flg15-sprayed
Treatment protocol After two weeks from transplanting, plants were sprayed with aqueous solutions of BP178 BP100 or flg 15 at 125 µM, SA and JA at 2.5 mM, to the run-off point.
Growth protocol Seeds of tomato plants cv. Rio Grande were sown in hydroponic seed plugs (rockwool), germinated and grown under controlled greenhouse conditions (25±2 ºC, 16 h light/ 15±2 ºC, 8 h dark, and 60% RH). Two-week old seedlings (two cotyledons) were transplanted into Rockwool plugs (7.5x7.5x6.5 cm).
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions after homogenization using TissueLyzerII system
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Tomato Gene 1.0 ST Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000
Data processing The microarray gene expression data was analyzed using GeneChip Expression Consol software (Affimetrix). Raw data (.cel files) were imported and processed, using Robust Multiarray Averaging (RMA) background correction, quantile normalization. Pre-processed data was analyzed by the web-base Babelomics (Medina et al., 2010) for gene expression analysis as the ratio of normalized fluorescence value between two compared treatments. This ration was then scaled using base 2 logarithm to obtain the log2 ratio, which in absolute terms is known as fold-change.
 
Submission date Sep 08, 2021
Last update date Sep 27, 2021
Contact name Emilio Montesinos
E-mail(s) emilio.montesinos@udg.edu
Phone (+34) 972418476
Organization name Universitat de Girona
Department INTEA
Lab Plant Pathology - CIDSAV
Street address c/Pic de Peguera, 15. PCiT. Edif. Jaume Casademont, porta E, 4t pis
City Girona
State/province Girona
ZIP/Postal code 17003
Country Spain
 
Platform ID GPL21525
Series (1)
GSE183707 Expression data from Solanum lycopersicum after elicitor molecules treatment

Data table header descriptions
ID_REF
VALUE Babelomics (Medina et al., 2010)

Data table
ID_REF VALUE
20190001 4.277179
20190003 4.077195
20190005 4.113236
20190007 5.02832
20190009 2.680529
20190011 3.975547
20190013 2.042928
20190015 1.971328
20190017 1.73722
20190019 2.505557
20190021 1.84028
20190023 2.246151
20190025 1.85844
20190027 2.370033
20190029 1.887412
20190031 2.144131
20190033 2.651787
20190035 1.858069
20190037 1.924969
20190039 1.813108

Total number of rows: 67795

Table truncated, full table size 1184 Kbytes.




Supplementary file Size Download File type/resource
GSM5568968_B27-31_TomGene-1_0-st_.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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