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Sample GSM2936536 Query DataSets for GSM2936536
Status Public on May 29, 2019
Title Root of control (untreated) Brassica napus, biological replicate 3
Sample type RNA
 
Source name Root of Brassica napus, left untreated for 4 days
Organism Brassica napus
Characteristics strain: Nourin No.16
agent: none
tissue: root
growth stage: 4 weeks after germination
Treatment protocol Plants were exposed to glutathione for 4 days. GSH (glutathione, reduced form) was applied to source leaves (fully expanded leaves). In the leaf GSH treatment, 50 µL of 100 mM GSH in a foliar-application solution (10 mM MES-KOH, pH6.1, 0.01% [w/v] Triton X-100) was applied to each leaf with a painting brush; GSH was applied to 3 expanded leaves per plant daily before harvest.
Growth protocol Seeds of oilseed rape (Brassica napus L. cv. Nourin No.16, Kaneko Seed Co. Ltd., Gumma, Japan) were germinated in vermiculite by using bottom irrigation. Modified Hoagland solution (nutrient solution), described previously [Soil Sci. Plant Nutr. 54 (2008) 118–127.], was used as the irrigation solution. At 10 days after germination, young seedlings were transferred to 1.5-L containers (4 seedlings/container) containing 1.2 L of the nutrient solution, and the containers were maintained in a growth chamber for a 16-h photoperiod (~200μmol m-2s-1) at 24 °C, and at 16°C at night. Nutrient solutions were aerated continuously and renewed twice weekly. Each tested plant was grown for 4 weeks before being harvested.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using an RNeasy Plant kit (Qiagen K.K., Tokyo, Japan).
Label biotin
Label protocol Biotinylated cRNA was obtained from 100 ng of purified total RNA using a GeneChip 3’ IVT Express Kit (Affymetrix, Santa Clara, CA, USA).
 
Hybridization protocol Following fragmentation, 12.5 µg cRNA were hybridized for 16 hr at 45°C on Affymetrix GeneChip Arabidopsis ATH1 Genome Array. GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
Description No additional information
Data processing CEL files were quantified with Distribution Free Weighted method (DFW), using the statistical language R (R-2.7.2) and Bioconductor 2.2.
 
Submission date Jan 17, 2018
Last update date May 29, 2019
Contact name Yuji Nakai
Organization name Hirosaki University
Department Institute of Regional Innovation
Lab Section of Food Sciences
Street address 2-1-1, Yanagawa
City Aomori
State/province Aomori
ZIP/Postal code 038-0012
Country Japan
 
Platform ID GPL198
Series (1)
GSE109282 Effect of foliar GSH treatment on gene expression profile in the root of Brassica napus

Data table header descriptions
ID_REF
VALUE DFW summarized signal

Data table
ID_REF VALUE
244901_at 5.559005756
244902_at 5.545588737
244903_at 5.740724939
244904_at 5.970772888
244905_at 5.628240149
244906_at 5.931032202
244907_at 5.497510938
244908_at 5.60565252
244909_at 5.903592827
244910_s_at 5.704465143
244911_at 5.358409387
244912_at 8.321192575
244913_at 5.820117322
244914_at 5.407815562
244915_s_at 5.74208252
244916_at 5.792495208
244917_at 5.650358284
244918_at 5.567180088
244919_at 6.053863186
244920_s_at 6.486507472

Total number of rows: 22810

Table truncated, full table size 490 Kbytes.




Supplementary file Size Download File type/resource
GSM2936536_C3.CEL.gz 1.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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