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Sample GSM528487 Query DataSets for GSM528487
Status Public on Apr 01, 2010
Title Treated 1
Sample type RNA
 
Source name curcumin treated Y79 cells
Organism Homo sapiens
Characteristics cell type: Y79 retinoblastoma cells
Treatment protocol Y79 cells were treated with 20uM curcumin for 48hrs.
Extracted molecule total RNA
Extraction protocol Total RNA extracted using using mirVana miRNA Isolation kit (Ambion, AM1560) following manufacturer's instructions
Label Cy3
Label protocol miRNA labeling was performed as described in Agilent miRNA microarray protocol version 2.0 using Agilent miRNA labeling kit. 100 ng of total RNA was dephosphorylated with calf intestine alkaline phosphatase for 30 min at 37°C. Denaturation was performed by adding DMSO and incubating at 100°C for 7 min and immediately transferred to ice water bath. Ligation was performed with pCp-Cy3 at 16 °C for 2 h. The labeled samples were dried completely in a vaccum concentrator and resuspended in 18 ul of nuclease free water.
 
Hybridization protocol The hybridization mixture [10X GE blocking agent (4.5 ul), 2X Hi-RPM hybridization buffer (22.5ul)] along with labeled miRNA sample was heated for 5 min at 100 °C and immediately cooled to 0 °C. Each 45 mL sample was hybridized onto a microarray at 55 °C for 20 h. Slides were washed 5 min in GE wash buffer 1 at RT and again for 5 min in GE wash buffer 2 at 37 °C, followed by an acetonitrile wash for 1 min at RT to dry the slides completely.
Scan protocol Scanned on an Agilent G2505C scanner and Images were quantified using Agilent Feature Extraction Software (version 10.5.1.1)
Description curcumin treated Y79 cells
Data processing The normalization was done using GeneSpring GX 11 Software. Recommended Percentile Shift Normalization and samples normalized with respect to control samples. Significant miRNA’S up and down regulated showing one fold and above among the groups was identified. Differentially regulated miRNA were clustered using hierarchical clustering to identify significant expression patterns. Using GeneSpring software miRNA targets was identified.
 
Submission date Mar 30, 2010
Last update date Mar 30, 2010
Contact name Genotypic technology
E-mail(s) sudha.rao@genotypic.co.in
Organization name Genotypic Technology
Street address 259, Apoorva 4th cross,80 feet Road,RMV 2ND STAGE
City Bangalore
State/province Karnataka
ZIP/Postal code 560094
Country India
 
Platform ID GPL7731
Series (1)
GSE21126 Y79 retinoblastoma cells: control vs. curcumin treated

Data table header descriptions
ID_REF
VALUE Normalized signal intensity (GeneSpring)
gProcessedSignal

Data table
ID_REF VALUE gProcessedSignal
1 0.18680763 2.02E+03
2 -0.8857858 6.40E+00
3 1.300262 1.78E+01
4 1.9630153 6.29E+00
5 -0.39124942 1.16E+01
6 -0.9282756 4.40E+00
7 -1.4555793 -1.40E+00
8 -0.69004464 -2.67E+00
9 2.1798267 7.31E+00
10 -3.4015396 -7.76E-01
11 -0.69004464 -7.13E+00
12 -1.3499694 -9.19E-01
14 2.0825448 1.64E+01
15 -1.6007774 -1.36E+00
16 -0.44032454 3.02E+00
17 -1.183692 3.75E+00
18 0.61752796 2.50E+01
19 0.33661556 1.42E+01
20 0.75953126 1.24E+01
21 0.6557305 4.88E+02

Total number of rows: 13737

Table truncated, full table size 348 Kbytes.




Supplementary file Size Download File type/resource
GSM528487_US83000164_251911812772_S01_miRNA_105_Dec08_1_2.txt.gz 1.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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