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Sample GSM184898 Query DataSets for GSM184898
Status Public on Apr 24, 2008
Title Arabidopsis, root cells, endodermis and quiescent center, standard conditions, replicate 1
Sample type RNA
Source name Protoplasted and FACS sorted root cells
Organism Arabidopsis thaliana
Characteristics Ecotype: Columbia
Age: Seedling roots, 6 days after germination
GFP-reporter: SCR::GFP
Growth Media: Standard media
Treatment protocol Samples were prepared as in Birnbaum et al. (2005) for roots grown under standard conditions. For salt treated samples, roots were transferred to 140 mM NaCl for 1hr before protoplasting. Three replicates were performed per cell type, per condition. In order to test for the effects of sorting, Col-0 roots were protoplasted after being treated for 1 hour with or without salt treatment. Cells were passed through the FACS device with all cells being collected.
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 at a density of ~20 seeds/cm in two rows.
Extracted molecule total RNA
Extraction protocol 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 isolated endodermal and quiecent center cells
Data processing MAS 5
Submission date Apr 26, 2007
Last update date Aug 28, 2018
Contact name Jose Ramon Dinneny
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)
GSE7641 Expression analysis of root cell-types after treatment with salt
Reanalyzed by GSE118579
Reanalyzed by GSE119083

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

Data table
AFFX-BioB-5_at 108.849 P 0.000856509
AFFX-BioB-M_at 163.036 P 4.42873e-05
AFFX-BioB-3_at 107.738 P 0.000224668
AFFX-BioC-5_at 365.695 P 5.16732e-05
AFFX-BioC-3_at 389.652 P 5.16732e-05
AFFX-BioDn-5_at 853.855 P 4.42873e-05
AFFX-BioDn-3_at 1656.34 P 5.16732e-05
AFFX-CreX-5_at 5288.51 P 4.42873e-05
AFFX-CreX-3_at 9025.56 P 4.42873e-05
AFFX-DapX-5_at 14.5827 A 0.175328
AFFX-DapX-M_at 1.29453 A 0.945787
AFFX-DapX-3_at 1.87557 A 0.891041
AFFX-LysX-5_at 9.69953 A 0.382599
AFFX-LysX-M_at 3.09107 A 0.659339
AFFX-LysX-3_at 1.54923 A 0.645547
AFFX-PheX-5_at 1.2159 A 0.989683
AFFX-PheX-M_at 1.32591 A 0.876428
AFFX-PheX-3_at 9.8811 A 0.425962
AFFX-ThrX-5_at 2.17938 A 0.843268
AFFX-ThrX-M_at 15.8825 A 0.227636

Total number of rows: 22810

Table truncated, full table size 676 Kbytes.

Supplementary file Size Download File type/resource
GSM184898.CEL.gz 3.3 Mb (ftp)(http) CEL
GSM184898.CHP.gz 123.4 Kb (ftp)(http) CHP
Raw data provided as supplementary file
Processed data provided as supplementary file

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