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Sample GSM814810 Query DataSets for GSM814810
Status Public on Dec 26, 2012
Title Prior oxidative stress to cold stress 3
Sample type RNA
 
Source name Prior oxidative stress to cold stress 3
Organism Oryza sativa Indica Group
Characteristics cultivar: Pusa Basmati (PB1)
age: 10-days old
tissue: whole seedling
oxidative stress: prior oxidative stress
temperature stress: cold stress
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)
PO_CS3
Prior oxidative stress to cold stress replicate 3
Agilent Feature Extraction file
US83000164_251524111359_S01_GE1_105_Dec08_1_2.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) anil.anilgrover@gmail.com
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|0 221.63
Os01g0100200|mRNA|AK059894|CDS+3'UTR 28.06
Os01g0100400|mRNA|AK101455|CDS+3'UTR 141.06
Os01g0100500|mRNA|AK067316|CDS+3'UTR 1731.34
Os01g0100600|mRNA|AK121362|CDS+3'UTR 511.32
Os01g0100700|mRNA|AK059844|CDS+3'UTR 8110.98
Os01g0100700|mRNA|AK121523|CDS+3'UTR 2376.36
Os01g0100800|mRNA|AK122012|CDS+3'UTR 1065.70
Os01g0100900|COMBINER_EST|CI015509|0 6910.10
Os01g0101200|mRNA|AK067866|CDS+3'UTR 336.33
Os01g0101200|mRNA|AK104517|CDS+3'UTR 1249.41
Os01g0101200|mRNA|AK104625|CDS+3'UTR 1341.30
Os01g0101200|mRNA|AK104752|CDS+3'UTR 1271.60
Os01g0101200|mRNA|AK119457|CDS+3'UTR 24.82
Os01g0101300|COMBINER_EST|CI016681|6 573.99
Os01g0101600|mRNA|AK099952|CDS+3'UTR 58.46
Os01g0101600|mRNA|AK103820|CDS+3'UTR 1371.37
Os01g0101600|mRNA|AK122118|CDS+3'UTR 1435.42
Os01g0101700|COMBINER_EST|CI525185|3 699.90
Os01g0101800|mRNA|AK103498|CDS+3'UTR 113.08

Total number of rows: 42418

Table truncated, full table size 1805 Kbytes.




Supplementary file Size Download File type/resource
GSM814810.txt.gz 7.8 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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