NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1210854 Query DataSets for GSM1210854
Status Public on Dec 31, 2015
Title HighCO2_6H_rep4
Sample type RNA
 
Source name HighCO2_6H_in_ChamberB
Organism Arabidopsis thaliana
Characteristics cultivar: Col-0; wild type
tissue: 14-d-old seedlings
exposed to: elevated (780 μmol mol-1) CO2 for 6hr
chamber id: ChamberB
Extracted molecule total RNA
Extraction protocol Approximately 500 μg of total RNA was three times extracted from each sample using TRIzol (Invitrogen).
Label Cy3
Label protocol cRNA amplification and fluorescence labeling were performed using the Agilent Low RNA Input Linear Amplification Kit (Agilent Technology, Tokyo, Japan) according to the manufacturer's protocol. A primer containing poly dT and a T7 polymerase promoter was annealed to the poly A+ RNA. First and second strands of cDNA were reverse transcribed from 500 ng total RNA using MMLV-RT enzyme. Cyanine 3- labeled cRNA was synthesized using T7 RNA polymerase. Labeled cRNA was purified by RNeasy Mini Kit (Qiagen, Tokyo, Japan).
 
Hybridization protocol Hybridization was performed using the in situ Hybridization Kit Plus (Agilent Technologies, Tokyo, Japan)
Scan protocol Hybridized and washed material on each glass slide was scanned by an Agilent G2505 B DNA microarray scanner (Agilent Technologies)
Description HighCO2_6H.b2
Data processing Data analysis was performed by Feature Extraction and Image Analysis software (Agilent Technologies, Tokyo, Japan).
The array intensities were processed using the Bioconductor (www.bioconductor.org) affy package in the R software environment (www.r-project.org). Hybridization intensities in our arrays were simply normalized among different arrays by quantile normalization.
 
Submission date Aug 18, 2013
Last update date Dec 31, 2015
Contact name Kousuke Hanada
E-mail(s) kohanada@bio.kyutech.ac.jp
Organization name Kyushu Institute Technology
Department Department of Bioscience and Bioinformatics
Street address 680-4 Kawazu
City Iizuka
State/province Fukuoka
ZIP/Postal code 820-8502
Country Japan
 
Platform ID GPL14937
Series (1)
GSE49960 Transcriptome analysis of annotated coding genes and sORF under elevated CO2

Data table header descriptions
ID_REF
VALUE quantile normalized

Data table
ID_REF VALUE
ATRIKEN31987 6.323279219
ATRIKEN13566 4995.815969
ATRIKEN08029 4.644677125
ATRIKEN27822 3.195491094
ATRIKEN27713 3.187857656
ATRIKEN10969 3.18186575
ATRIKEN20199 20200.07375
ATRIKEN30075 3.168748938
ATRIKEN30830 3.170321125
ATRIKEN07335 1190.733322
ATRIKEN13579 1244.995963
ATRIKEN14133 649.4950938
ATRIKEN11487 93.60045906
ATRIKEN20010 1694.686547
ATRIKEN12111 1245.859563
ATRIKEN17481 7.975087969
ATRIKEN03251 852.9877906
ATRIKEN01799 8651.021344
ATRIKEN23687 4139.294063
ATRIKEN21530 23.511465

Total number of rows: 34262

Table truncated, full table size 830 Kbytes.




Supplementary file Size Download File type/resource
GSM1210854_252283010085_1HighCO2-6hr-4.txt.gz 6.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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