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Sample GSM261047 Query DataSets for GSM261047
Status Public on Apr 29, 2009
Title after 3 days in mannitol medium rep3
Sample type RNA
Source name 100904A_DH46_4d4
Organism Hordeum vulgare
Characteristics after 3 days in mannitol medium
Treatment protocol Anthers extracted from the spikes under a stereoscopic microscope were inoculated in a treatment medium containing 0.7 M mannitol, 40 mM CaCl2, and 8 g/l agarose, and kept at 25 C in the dark for 4 days (Cistue´et al. 2003). Samples were collected before and after 4 days in mannitol medium. Three samples from each step were harvested and used for microarray analysis.
Growth protocol Donor plants were grown in growth chambers with controlled temperature (18-21ºC), relative humidity (70-80%) and photoperiod (16 h light), as described by Cistué et al. (2003).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIzol reagent (Invitrogen) from frozen crown samples taken from above soil tissue excluding most fully extended lamina. The protocol is available on the Arabidopsis Information Resource website at RNA was purified using Qiagen RNeasy spin columns with DNase treatment. Quality was assessed by running 25-250 ng on a RNA Lab-On-A-Chip (Caliper Technologies) using an Agilent Bioanalyzer 2100 (Agilent Technologies).
Label biotin
Label protocol The BioArray High-Yield RNA Transcript Labeling Kit (Enzo Diagnostics) was then used to synthesize biotin-labeled cRNA from template cDNA by in vitro transcription.
Hybridization protocol 10 µg labeled, fragmented cRNA was hybridized at 45°C with rotation for 16 hours in an Affymetrix GeneChip Hybridization Oven 320 on Affymetrix Barley1 Genechip arrays. The arrays were washed and stained using streptavidin phycoerythrin on an Affymetrix Fluidics Station 400.
Scan protocol The arrays were scanned on a Hewlett-Packard GeneArray scanner.
Description after 3 days in mannitol medium
Data processing GCOS MAS 5
Submission date Jan 30, 2008
Last update date Apr 28, 2009
Contact name Livia Tommasini
Phone 951 827 3808
Fax 951 827 4437
Organization name University of California, Riverside
Department Botany and Plant Science
Lab Tim Close
Street address 2150 Batchelor Hall
City Riverside
State/province CA
ZIP/Postal code 92521-0124
Country USA
Platform ID GPL1340
Series (1)
GSE10330 Transcriptome analysis of barley anthers: effect of mannitol treatment on microspore embryogenesis

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 127.388 P 0.00179591
AFFX-BioB-M_at 119.991 P 0.000258358
AFFX-BioB-3_at 75.0112 P 0.00556451
AFFX-BioC-5_at 322.484 P 9.4506e-05
AFFX-BioC-3_at 478.381 P 4.42873e-05
AFFX-BioDn-5_at 821.441 P 5.16732e-05
AFFX-BioDn-3_at 1860.2 P 9.4506e-05
AFFX-CreX-5_at 3852.44 P 4.42873e-05
AFFX-CreX-3_at 8485.68 P 4.42873e-05
AFFX-DapX-5_at 50.2495 P 0.0138105
AFFX-DapX-M_at 209.424 P 0.000753643
AFFX-DapX-3_at 409.273 P 9.4506e-05
AFFX-LysX-5_at 17.6919 A 0.227636
AFFX-LysX-M_at 44.8817 A 0.262827
AFFX-LysX-3_at 131.129 P 0.000445901
AFFX-PheX-5_at 19.2388 A 0.156732
AFFX-PheX-M_at 9.16127 A 0.58862
AFFX-PheX-3_at 73.4326 P 0.00320999
AFFX-ThrX-5_at 30.6044 A 0.156732
AFFX-ThrX-M_at 59.109 M 0.050229

Total number of rows: 22840

Table truncated, full table size 792 Kbytes.

Supplementary file Size Download File type/resource
GSM261047.CEL.gz 2.2 Mb (ftp)(http) CEL
GSM261047.CHP.gz 122.6 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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