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Sample GSM1346430 Query DataSets for GSM1346430
Status Public on Feb 26, 2015
Title Fatbody_UV12h_sample2
Sample type RNA
 
Source name fatbody, 3 day of fifth instar larvae, domestic silkworm, Kinshu x Showa
Organism Bombyx mori
Characteristics tissue: fatbody
developmental stage: 3day fifth instar larvae
stress: UV
time: 12h
Treatment protocol Silkworms were reared on fresh mulberry leaves and kept at 25 degrees Celsius on a 12-hour light/12-hour dark cycle.
Extracted molecule total RNA
Extraction protocol Total RNA from control or UV treated fatbody were isolated using an RNeasy Mini Kit (Qiagen, Valencia, CA, USA). Total RNA was quantified on an Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA)
Label Cy3
Label protocol Total RNA(300ng) was processed for Cy3-labelled cRNA synthesis using the Agilent Quick Amp Labeling Kit according to the manufacturer's instructions (Agilent Technologies). The Cy3-labelled cRNA was purified using RNeasy Mini Kit (Qiagen) and quantified on an Agilent 2100 and Nano Drop 1000 Spectrophotometer.
 
Hybridization protocol Hybridization was performed using the Gene Expression Hybridization Kit (Agilent Technologies). 1.65ug of Cy3-labelled cRNA was mixed, fragmented and hybridized to the silkworm 4 x 44 K oligo-microarray slide at 65 degrees Celsius for 17 hours with shaking at 10 rpm. The array was washed in Agilent Gene Expression Wash Buffer 1 for 1min at room temperature and Agilent Gene Expression Wash Buffer 2 for 1min at 37 degrees Celsius.
Scan protocol Intensities of the hybridized probes were detected with an Agilent G2565B Microarray Scanner at 10-mm scan resolution.
Description Gene expression in 3day fifth instar larvae of UV treatment for 12 hours
Data processing Signals were extracted with G2565AA Feature Extraction Software v.9.5 (Agilent Techonologies). The raw data in text files were normalized 'per spot' and 'per chip' using GeneSpring GX v.10.3 (Agilent Techonologies).
 
Submission date Mar 12, 2014
Last update date Feb 26, 2015
Contact name Hiromasa Ono
E-mail(s) hono@dbcls.rois.ac.jp
Organization name Research Organization of Information and Systems
Department Database Center for Life Science (DBCLS)
Lab Mishima Lab.
Street address National Institute of Genetics, Yata 1111
City Mishima
State/province Shizuoka
ZIP/Postal code 411-8540
Country Japan
 
Platform ID GPL15525
Series (1)
GSE55816 Gene expression of ultra violet irradiation of silk worm Bombyx mori larvae

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
Ka14571_559 -0.07055187
Ka05841_1 0.20328331
Ka25297_791 -0.24941492
Ka05841_21 -0.045166492
Ka17145_220 -0.33723164
Ka06133_667 -0.12138367
Ka06133_308 0.22495937
Ka05329_102 0.27467537
Ka25657_532 0.3036251
Ka16732_324 1.0088744
Ka05329_199 0.1426816
Ka20861_623 -0.22272396
Ka17116_72 0.26107073
Ka05817_225 0.21367836
Ka13371_404 -0.79582906
Ka05817_408 0.23142195
Ka29575_437 0.09861612
Ka22842_289 0.7697995
Ka20928_1 0.6998863
Ka06453_263 1.7394853

Total number of rows: 43848

Table truncated, full table size 994 Kbytes.




Supplementary file Size Download File type/resource
GSM1346430_Fatbody_UV12h_sample2.txt.gz 1.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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