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Sample GSM243270 Query DataSets for GSM243270
Status Public on Jan 30, 2008
Title Transcriptome analyses of HeLa cells treated by CTCF RNAi(1)
Sample type RNA
 
Source name HeLa cells treated by CTCF RNAi
Organism Homo sapiens
Characteristics HeLa cells treated by CTCF RNAi was used.
Extracted molecule total RNA
Extraction protocol The siRNA oligos were annealed according to manufacturer’s instruction and used at a final concentration of 100-200 nM. The siRNA transfection was performed using oligofectamine (Invitrogen) and the cells were synchronized in G2 phase by double thymidine block before harvesting. For the preparation of total RNA from mammalian cells, Trizol extraction protocol was used, followed by a clean up step using the RNeasy Total RNA Isolation Mini Kit (Qiagen 74104).To minimize the possibility of artifacts by RNAi treatment, experiment was performed twice, using two different oligos for the knock down of hScc1 and CTCF, respectively.
Label biotin
Label protocol IVT labelling was performed using GeneChip Expression 3'-Amplification Reagents (P/N900449)
 
Hybridization protocol Samples were denatured at 99C for 5 minutes, and then put at 45C for 5min. before being hybridized for 16 hours at 45C in an hybridization oven (GeneChip Hybridization Oven 640, Affymetrix). Washing and scanning protocol provided by Affymetrix was performed automatically on a fluidics station (GeneChip fluidics station 450, Affymetrix).
Scan protocol Arrays were scanned using the Genechip Scanner3000 7G following the library array description.
Description Transcriptome analyses of HeLa cells treated by CTCF RNAi(1). CTCF RNAi sample was compared with non-treated control RNAi sample(ControlRNAi(1)).
Data processing Chip data was analyzed by MAS (Microarray Analysis Suit) 5 software provided by Affymetrix using default setting.
 
Submission date Nov 16, 2007
Last update date Aug 28, 2018
Contact name Katsuhiko Shirahige
E-mail(s) [email protected]
Phone +81-3-5842-0756
Fax +81-3-5842-0757
URL http://www.iam.u-tokyo.ac.jp/chromosomeinformatics/
Organization name The University of Tokyo
Department Research Center for Epigenetic Disease
Lab Laboratory of Genome Structure and Function
Street address 1-1-1 Yayoi
City Bunkyo-ku
State/province Tokyo
ZIP/Postal code 113-0032
Country Japan
 
Platform ID GPL570
Series (1)
GSE9613 Cohesin mediates transcriptional insulation by CCCTC-binding factor
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
Raw Signal Intensity MAS5.0-calculated Signal Intensity
VALUE Normalized Signal Intensity against control RNAi
Fold Change Signal Log Ratio
Change Call
Change P-value

Data table
ID_REF Raw Signal Intensity VALUE Fold Change Change Call Change P-value
AFFX-BioB-5_at 173.5 162.8 -0.1 NC 0.801447
AFFX-BioB-M_at 216 202.7 -0.3 D 0.999921
AFFX-BioB-3_at 136.1 127.8 -0.2 D 0.999825
AFFX-BioC-5_at 374.5 351.4 -0.3 MD 0.997619
AFFX-BioC-3_at 506.6 475.4 -0.3 D 0.999921
AFFX-BioDn-5_at 1487.4 1395.8 -0.3 D 0.999995
AFFX-BioDn-3_at 3155.3 2960.9 -0.3 D 0.999997
AFFX-CreX-5_at 6972.1 6542.7 -0.2 D 0.999664
AFFX-CreX-3_at 8307.4 7795.7 -0.2 D 0.999999
AFFX-DapX-5_at 139.7 131.1 -1.3 D 1
AFFX-DapX-M_at 416 390.4 -1.1 D 1
AFFX-DapX-3_at 716.7 672.5 -1.1 D 1
AFFX-LysX-5_at 43.4 40.8 -1.3 D 1
AFFX-LysX-M_at 75.3 70.6 -1.1 D 0.999992
AFFX-LysX-3_at 146.3 137.3 -1 D 1
AFFX-PheX-5_at 53.3 50 -1.3 D 1
AFFX-PheX-M_at 53.1 49.9 -1 D 0.999999
AFFX-PheX-3_at 77.5 72.7 -1.1 D 1
AFFX-ThrX-5_at 48.2 45.2 -1.2 D 1
AFFX-ThrX-M_at 84.4 79.2 -1.3 D 1

Total number of rows: 54675

Table truncated, full table size 1869 Kbytes.




Supplementary file Size Download File type/resource
GSM243270.CEL.gz 4.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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