GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Sample GSM261068 Query DataSets for GSM261068
Status Public on Apr 29, 2009
Title Albina f-17 Control rep1
Sample type RNA
Source name 5
Organism Hordeum vulgare
Characteristics Albina f-17 Control
Treatment protocol When the first leaf was fully emerged the plants were treated for 6 d at 3 C, 12-h light (150 mmol m22 s21)/1 C, 12-h dark. Control plants were harvested after 8 d at 20 C. All samples were collected in the middle of the light period. This experiment was conducted three times to yield three independent biological replicates. To analyze the involvement of the photooxidative stress, seeds of wild type and mutants were imbibed for 3 h in water containing 0 (control) or 50 mM norfluorazon. The hydrated seeds were grown in a growth-controlled environment chamber as above except that light intensity was 10 mmol m22 s21 for the first 8 d and 200 mmol m22 s21 for the next 6 d. During the growth, treated plants were watered two times with 50 mM norfluorazon.For analysis of Cbf expression, treated samples were collected after 4, 8, and 24 h of cold treatment in the light.
Growth protocol Wild type and mutants were germinated in peat pots and grown in a controlled-environment chamber for 8 d at 20 C with 12-h photoperiod (300 mmol m22 s21).
Extracted molecule total RNA
Extraction protocol For RNA isolation, two methods were applied: RNA from embryo and endosperm collected during seed development was isolated by Trizol (Gibco BRL Life Technologies, Rockville, MD) and passed through an RNeasy spin column (Qiagen, Hilden, Germany) for further clean up as recommended by Affymetrix, Inc. (Affymetrix GeneChip Expression Analysis Technical Manual, Affymetric, Inc., Santa Clara, CA). For embryo and endosperm collected after imbibition, PURESCRIPT® RNA isolation kits (Gentra Systems, Inc., Minneapolis, MN) and RNeasy spin column (Qiagen, Hilden, Germany) were used. Quality of RNA was assessed on an Agilent Bioanalyzer 2100 (Agilent Technologies, Palo Alto, CA).
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 Albina f-17 Control
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)
GSE10332 Transcriptome Analysis of Cold Acclimation in Barley Albina and Xantha Mutants1

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 195.51 P 0.00844047
AFFX-BioB-M_at 155.341 P 0.000972149
AFFX-BioB-3_at 159.694 P 0.00359458
AFFX-BioC-5_at 391.113 P 0.00141043
AFFX-BioC-3_at 342.694 P 0.000856509
AFFX-BioDn-5_at 315.363 P 0.00010954
AFFX-BioDn-3_at 2673.01 P 0.000146581
AFFX-CreX-5_at 4839.72 P 4.42873e-05
AFFX-CreX-3_at 9708.96 P 4.42873e-05
AFFX-DapX-5_at 25.935 A 0.250796
AFFX-DapX-M_at 26.2652 A 0.205732
AFFX-DapX-3_at 6.12781 A 0.824672
AFFX-LysX-5_at 2.70371 A 0.737173
AFFX-LysX-M_at 18.4953 A 0.724854
AFFX-LysX-3_at 17.1137 A 0.455413
AFFX-PheX-5_at 3.90997 A 0.772364
AFFX-PheX-M_at 3.13613 A 0.876428
AFFX-PheX-3_at 12.9905 A 0.883887
AFFX-ThrX-5_at 6.08228 A 0.941556
AFFX-ThrX-M_at 41.8146 A 0.368438

Total number of rows: 22840

Table truncated, full table size 785 Kbytes.

Supplementary file Size Download File type/resource
GSM261068.CEL.gz 3.5 Mb (ftp)(http) CEL
GSM261068.CHP.gz 6.2 Mb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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