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Sample GSM184934 Query DataSets for GSM184934
Status Public on Apr 24, 2008
Title Arabidopsis, whole roots, 140 mM NaCl, 16 hour, replicate 2
Sample type RNA
 
Source name whole roots
Organism Arabidopsis thaliana
Characteristics Ecotype: Columbia
Age: Seedling roots, 5 days after germination
Growth Media: Standard media for 4 days then transferred to media supplemented with 140 mM NaCl
Treatment length: 16 hours
Treatment protocol Seedlings were grown for 4-5 days before transfer to standard media supplemented with 140 mM NaCl. Transfers were staggered such that all roots were harvested within 3 hours of each other on the sixth day of growth. Roots were cut with a razor blade 0.5 mm below the root/hypocotyl junction and collected into RNA extraction buffer. Approximately 15 roots were collected per replicate, with two biological replicates being performed per time point. Samples were briefly sonicated to disrupt the tissue.
Growth protocol Seeds were surface sterilized with 50% Bleach and 0.1% Tween for 5 minutes and then rinsed 3 times with sterile water. Seeds were stratified at 4˚C for 2 days before being planted on standard media. Standard media is 1X concentration Murashige and Skoog salt mixture (Caisson laboratories), 0.5g/L MES, 1% sucrose, 1% agar and adjusted to pH 5.7 with KOH. Salt media is standard media with varying amounts of NaCl added. Nylon mesh was placed on top of the solidified media and seeds were evenly placed on the mesh in a single row at a density of ~2/cm for all experiments.
Extracted molecule total RNA
Extraction protocol Approximately 15 roots were collected per replicate. Samples were briefly sonicated to disrupt the tissue. RNA was extracted using the RNAeasy Micro Kit (Qiagen GmbH).
Label biotin
Label protocol Fragmented cRNA probes were prepared using the two-cycle amplification protocol by Affymetrix.
 
Hybridization protocol Standard Affymetrix protocols. Samples were submitted to Expression Analysis Inc. (Durham, NC) for hybridization to Affymetrix ATH1 microarrays.
Scan protocol Standard Affymetrix protocols. Samples were submitted to Expression Analysis Inc. (Durham, NC) for hybridization to Affymetrix ATH1 microarrays.
Description Gene expression data from whole roots grown under standard conditions for 5 days and transferred to media supplemented with 140 mM NaCl for 16 hours
Data processing MAS 5
 
Submission date Apr 26, 2007
Last update date Aug 28, 2018
Contact name Jose Ramon Dinneny
E-mail(s) [email protected]
Organization name Carnegie Institution for Science, Department of Plant Biology
Department Plant Biology
Lab Jose R. Dinneny
Street address 260 Panama St
City Stanford
State/province United States
ZIP/Postal code 94305
Country USA
 
Platform ID GPL198
Series (1)
GSE7642 Time course expression analysis of the salt stress response in Arabidopsis roots
Relations
Reanalyzed by GSE118579
Reanalyzed by GSE119083

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 130.509 P 0.000195116
AFFX-BioB-M_at 194.483 P 7.00668e-05
AFFX-BioB-3_at 100.102 P 7.00668e-05
AFFX-BioC-5_at 350.343 P 4.42873e-05
AFFX-BioC-3_at 292.534 P 4.42873e-05
AFFX-BioDn-5_at 809.344 P 4.42873e-05
AFFX-BioDn-3_at 1237.46 P 4.42873e-05
AFFX-CreX-5_at 4443.3 P 4.42873e-05
AFFX-CreX-3_at 4882.56 P 4.42873e-05
AFFX-DapX-5_at 9.10583 M 0.0542134
AFFX-DapX-M_at 1.20145 A 0.876428
AFFX-DapX-3_at 0.463023 A 0.99238
AFFX-LysX-5_at 0.874359 A 0.834139
AFFX-LysX-M_at 1.7164 A 0.945787
AFFX-LysX-3_at 3.55529 A 0.544587
AFFX-PheX-5_at 0.758076 A 0.984817
AFFX-PheX-M_at 0.873767 A 0.9273
AFFX-PheX-3_at 2.5716 A 0.712257
AFFX-ThrX-5_at 0.645552 A 0.960339
AFFX-ThrX-M_at 1.25043 A 0.772364

Total number of rows: 22810

Table truncated, full table size 683 Kbytes.




Supplementary file Size Download File type/resource
GSM184934.CEL.gz 3.4 Mb (ftp)(http) CEL
GSM184934.CHP.gz 122.7 Kb (ftp)(http) CHP
Processed data provided as supplementary file

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