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Sample GSM814819 Query DataSets for GSM814819
Status Public on Dec 26, 2012
Title Control 3
Sample type RNA
 
Source name Control 3
Organism Oryza sativa Indica Group
Characteristics cultivar: Pusa Basmati (PB1)
age: 10-days old
tissue: whole seedling
oxidative stress: control
temperature stress: control
Treatment protocol For oxidative Stress prior to High Temperature Stress (PO_HS) or Low Temperature Stress (PO_CS) uniformly grown seedlings (10 day old) were transferred to beakers, which contain 10mM H2O2 at 28+2oC for oxidative stress (OS) for 4 h and followed by heat stress (HS) 42+1oC for 30 minutes/ cold stress (HS) 5+1oC for 5 h in the growth chamber with lights on. Similarly for oxidative Stress during High Temperature Stress (DO_HS)/ during Low temperature stress (DO_CS) uniformly grown seedlings (10 day old) were transferred to beakers, which contain 10mM H2O2 maintained at 42+1oC for heat stress (HS) for 30 minutes/5+1oC for cold stress (CS) in the BOD with lights on. All Samples were harvested, frozen in liquid nitrogen and kept at -80°C immediately after stress treatment.
Growth protocol Seedlings were grown at 28+2oC and 14 h light/ 10 h dark cycle maintained in growth room (light intensity ~250µmol.m-2.s-2, humidity 40-50%) for 10 d.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from ~100 mg tissue using Tri- Reagent (Sigma, USA) as per the manufacturer’s instructions, and further purified using RNAesy Mini Elute Kit (Qiagen).
Label Cy3
Label protocol Total RNA (200ng) was labeled with Cy3 using Agilent Low RNA Input fluorescent Linear Amplification Kit (Agilent Technologies). Cyanine-3 (Cy3) labeled cRNA was prepared from 0.5 ug RNA using the One-Color Low RNA Input Linear Amplification PLUS kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol Hybridization and wash processes were performed according to the manufacturer’s instructions.
Scan protocol Hybridized microarrays were scanned using agilent microarray scanner (g2505b, agilent technologies, usa) at 5µ resolution.
Description Oryza sativa ssp. indica L; cultivar Pusa Basmati (PB1)
Cont3
Control replicate 3
Agilent Feature Extraction file
US83000164_251524111358_S01_GE1_105_Dec08_1_3.txt
Data processing Feature extraction software (version 10.5.1.1 Agilent Technologies, USA) was employed for the image analysis and data extraction process. The normalization was done using GeneSpring GX 10.2 (Agilent Technologies, USA) using the recommended Per Chip and Per Gene Data Transformation: Set measurements less than 0.01 to 0.01, Per Chip: Normalize to 50th percentile Per Gene: Normalize to Specific Samples (Treated Vs Control). Data analysis was done using GeneSpring GX version 7.3.1 (Agilent Technologies, USA) and Microsoft Excel. In total three biological replicates were processed in a similar manner for the microarray analysis. Genes showing differential expression (up or down) by 2 fold or more (log2 values) with a p- value less than or equal to 0.05 were considered statistically significant.
 
Submission date Oct 12, 2011
Last update date Dec 26, 2012
Contact name Anil Grover
E-mail(s) [email protected]
Phone 91-11-24117693
Fax 91-11-24115270
URL http://www.south.du.ac.in/dpmb/index.php?page=anil-grover
Organization name University of Delhi South Campus
Department Plant Molecular Biology
Lab Stress Biology Lab
Street address Benito Juarez Road
City New Delhi
State/province Delhi
ZIP/Postal code 110021
Country India
 
Platform ID GPL8852
Series (1)
GSE32704 Transcriptional changes in response to oxidative stress in combination with temperature extremes in rice

Data table header descriptions
ID_REF
VALUE gProcessedSignal (normalized) values from Agilent Feature Extraction files

Data table
ID_REF VALUE
Os01g0100100|COMBINER_EST|CI448596|0 655.47
Os01g0100200|mRNA|AK059894|CDS+3'UTR 49.89
Os01g0100400|mRNA|AK101455|CDS+3'UTR 590.81
Os01g0100500|mRNA|AK067316|CDS+3'UTR 4294.15
Os01g0100600|mRNA|AK121362|CDS+3'UTR 1705.68
Os01g0100700|mRNA|AK059844|CDS+3'UTR 26700.84
Os01g0100700|mRNA|AK121523|CDS+3'UTR 8448.41
Os01g0100800|mRNA|AK122012|CDS+3'UTR 1730.52
Os01g0100900|COMBINER_EST|CI015509|0 9600.88
Os01g0101200|mRNA|AK067866|CDS+3'UTR 1320.17
Os01g0101200|mRNA|AK104517|CDS+3'UTR 6157.31
Os01g0101200|mRNA|AK104625|CDS+3'UTR 6941.31
Os01g0101200|mRNA|AK104752|CDS+3'UTR 7284.46
Os01g0101200|mRNA|AK119457|CDS+3'UTR 51.94
Os01g0101300|COMBINER_EST|CI016681|6 703.19
Os01g0101600|mRNA|AK099952|CDS+3'UTR 307.53
Os01g0101600|mRNA|AK103820|CDS+3'UTR 2526.56
Os01g0101600|mRNA|AK122118|CDS+3'UTR 2467.14
Os01g0101700|COMBINER_EST|CI525185|3 2149.58
Os01g0101800|mRNA|AK103498|CDS+3'UTR 1080.41

Total number of rows: 42418

Table truncated, full table size 1815 Kbytes.




Supplementary file Size Download File type/resource
GSM814819.txt.gz 7.7 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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