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Sample GSM284631 Query DataSets for GSM284631
Status Public on May 15, 2008
Title Col-0_bud_totalRNA_R_1
Sample type RNA
 
Source name Immature floral tissue, unopened buds
Organism Arabidopsis thaliana
Characteristics Columbia-0
Treatment protocol no treatment
Growth protocol All plants were grown in potting soil (Metro Mix 250; Grace-Sierra, Boca Raton, FL) at 23C under a 16-hour light/8-hour dark cycle.
Extracted molecule total RNA
Extraction protocol total RNA was isolated from immature floral tissue following instructions from the manufacturer (Qiagen, RNeasy Plant Mini Kit).
Label biotin
Label protocol Fifteen micrograms of total RNA was used to synthesize double-stranded cDNA using the GeneChip One-Cycle cDNA Synthesis Kit (Affymetrix). Biotin-labeled cRNA was generated by in vitro transcription using the GeneChip IVT Labeling Kit (Affymetrix).
 
Hybridization protocol The Arabidopsis Tiling 1.0R whole genome tiling array was hybridized for 16 h, washed and stained with a streptavidin-phycoerythrin conjugate on the Affymetrix Fluidics Station 450 according to the standard Affymetrix protocol.
Scan protocol GeneChips were scanned on Affymetrix Scanner G7
Description Col-0 flower bud total RNA Reverse replicate 1
Data processing Gene chip data files were processed using TileMap to identify regions of significant changes in gene expression, with a cutoff of 0.6 pp.
 
Submission date Apr 25, 2008
Last update date Sep 24, 2010
Contact name Joseph R Ecker
E-mail(s) ecker@salk.edu
Phone 8584534100
Organization name HHMI-Salk-Institute
Department Genomic Analysis Laboratory
Lab Ecker lab
Street address 10010 North Torrey Pines Road
City La Jolla
State/province CA
ZIP/Postal code 92037
Country USA
 
Platform ID GPL10977
Series (1)
GSE11070 A link between RNA metabolism and silencing affecting Arabidopsis development

Supplementary file Size Download File type/resource
GSM284631.CEL.gz 40.7 Mb (ftp)(http) CEL
Processed data not provided for this record

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