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Sample GSM619288 Query DataSets for GSM619288
Status Public on Jan 15, 2012
Title Skov3 Flag P10
Sample type RNA
 
Source name Flag plasmid, passage #10
Organism Homo sapiens
Characteristics cell line: SKOV-3 cells
cell passage: P10
transfectant: Flag plasmid
Treatment protocol SKOV-3 cells were seeded one day before transfection with pCMV-Flag-Evi1 plasmid, pCMV-Flag plasmid, Evi1 siRNA (Evi1 ON-TARGETplus siRNA#8 plus #10) or control siRNA (ON-TARGETplus Non-targeting Pool, Dharmacon)
Growth protocol SKOV-3 cells (ATCC, HTB-77) were grown at 37degres in 10%FBS RPMI. They were passaged every 3-4 days. P8, P9, P10, P11 in the sample names refer to the cell passage number.
Extracted molecule total RNA
Extraction protocol total RNA was extracted with Trizol reagent, followed by clean-up and DNase I treatment with QIAGEN RNeasy mini kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with Agilent Bioanalyser.
Label biotin
Label protocol Biotinylated ss-cDNA were prepared with GeneChip WT cDNA synthesis and Amplification Kit, GeneChip WT terminal Labeling Kit and GeneChip Sample Cleanup Module (Affymetrix).
 
Hybridization protocol GeneChip Hybridization Control Kit and GeneChip Hybridization, Wash, Stain Kit (Affymetrix) were used to hybidize Human Gene 1.0ST arrays.
Scan protocol Standard Affymetrix Scan protocol was followed.
Data processing The data were analyzed with Partek Genomics Suite version 6.4 using Affymetrix default analysis settings and global scaling as normalization method.
 
Submission date Nov 09, 2010
Last update date Sep 01, 2016
Contact name Justin Jeyakani Joseph Gnanakkan
E-mail(s) [email protected]
Phone 68088173
Organization name Genome Institute of Singapore
Department Computational and Systems Biology
Street address 60, Biopolis street
City Singapore
State/province Singapore
ZIP/Postal code 138672
Country Singapore
 
Platform ID GPL6244
Series (2)
GSE25212 Effects of Evi1 knockdown and overexpression in SKOV-3 ovarian carcinoma cells
GSE25213 EVI1 and AP1 Interact to Transcriptionally Regulate a Feed-Forward Loop Important for Cancer Cell Proliferation and Adhesion
Relations
Reanalyzed by GSE86357

Data table header descriptions
ID_REF
VALUE GC-RMA signal intensity

Data table
ID_REF VALUE
7896736 6.30815
7896738 3.12566
7896740 3.40675
7896742 7.15853
7896744 5.68386
7896746 10.4928
7896748 11.8965
7896750 8.08324
7896752 11.5488
7896754 6.44835
7896756 5.19107
7896759 7.6453
7896761 8.23546
7896779 7.41526
7896798 7.56592
7896817 7.3896
7896822 9.17791
7896859 6.50971
7896861 4.11422
7896863 6.00512

Total number of rows: 28869

Table truncated, full table size 447 Kbytes.




Supplementary file Size Download File type/resource
GSM619288.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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