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Sample GSM2133236 Query DataSets for GSM2133236
Status Public on Apr 27, 2016
Title YO20mg_4
Sample type RNA
 
Source name Y2O3-treatment_20 mg, 8h, replicate4
Organism Saccharomyces cerevisiae
Characteristics strain: S288C
Treatment protocol After yeast cells were grown for 6 h (exponentially growing cells) at 30℃, 5 mg of YCl3・6H2O (Wako Pure Chemical Industries, Osaka, Japan) or 3 mg, 20 mg of Y2O3 nanoparticle (CIK NanoTek Corporation, Tokyo, Japan) were exposed to yeast cells, and these yeast cells were further incubated for 2h.
Growth protocol These yeast cells were grown in YPD medium (1.0% yeast extract, 2.0% peptone ; Becton, Dickinson and Co., NJ, USA, and 2.0% glucose, if necessary 1.5% agar; Wako Pure Chemical Industries, Ltd, Osaka, Japan) at 30°C for 8 h.
Extracted molecule total RNA
Extraction protocol The yeast cells after stressed were collected by centrifugation of 15,000 rpm for 1.0 min at 4°C. RNA extraction conformed according to partially modified manufacture protocol of Fast RNA ® Pro Red Kit (MP Biomedicals, CA, USA). RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3
Label protocol The cDNA was synthesized by Quick Amp Labeling Kit (Agilent) using 0.5 μg total RNA as a template. Cyanine-3 (Cy3) labeled cRNA was prepared from cDNA using the T7 RNA polymerase. Cy3-labeled cRNA was purified by RNeasy Mini Kit (QIAGEN, Hilden, Germany), and checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol Cy3-labelled cRNA was fragmented at 60°C for 30 min in a reaction volume of 25 μl containing 1x Blocking Agent and 1x Fragmentation Buffer. On completion of the fragmentation reaction, 2x Hybridization Buffer HI-RPM solution was added to the fragmentation mixture containing 0.6 μg of Cy3-labelled cRNA and hybridized for 17 h, at 65C and 10 rpm. After hybridization, microarrays were washed according to Quick Amp Labeling Kit Protocol (Agilent).
Scan protocol The hybridized microarray slides were washed according to the manufacturer’s instructions and were scanned with an Agilent DNA Microarray Scanner (#G2565CA, Agilent Technologies, CA, USA) at a resolution of 5 μm.
Data processing These data were normalized by the quantile methods using Excel.
 
Submission date Apr 26, 2016
Last update date Apr 27, 2016
Contact name Akihiro Moriyama
Organization name Gifu University
Street address 1-1, Yanagido
City Gifu
ZIP/Postal code 501-1193
Country Japan
 
Platform ID GPL16244
Series (1)
GSE80677 Gene expression profiles of yeast treated with YCl3 and Y2O3 nanoparticle

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
A_06_P1001 3468.562728
A_06_P1002 455.6615813
A_06_P1003 2234.17701
A_06_P1004 30.28153568
A_06_P1005 137.9209629
A_06_P1006 232.3221503
A_06_P1007 83.77767228
A_06_P1008 812.1531418
A_06_P1009 7584.096195
A_06_P1010 371.1018508
A_06_P1011 8642.194275
A_06_P1012 2851.662025
A_06_P1013 992.9448
A_06_P1014 8582.222418
A_06_P1015 21.1022735
A_06_P1016 7509.133138
A_06_P1017 1589.38907
A_06_P1018 318.1207685
A_06_P1019 2774.496768
A_06_P1020 27.4527518

Total number of rows: 6256

Table truncated, full table size 138 Kbytes.




Supplementary file Size Download File type/resource
GSM2133236_US11033868_251632210933_S01_GE1_107_Sep09_1_4.txt.gz 638.5 Kb (ftp)(http) TXT
Processed data included within Sample table

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