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Sample GSM756978 Query DataSets for GSM756978
Status Public on Oct 07, 2011
Title INS1 control, bioological rep2
Sample type RNA
 
Source name Insulinoma 832/13 INS-1 cell line
Organism Rattus norvegicus
Characteristics passage: between passages 7 and 25
cell line: Insulinoma 832/13 INS-1 cell line
treatment: scrambled
Treatment protocol COUP-TFII depletion experiments in the 832/13 INS-1 cell line were performed as described previously (Perilhou A, Tourrel-Cuzin C, Kharroubi I, Henique C, Fauveau V, Kitamura T, Magnan C, Postic C, Prip-Buus C, Vasseur-Cognet M (2008). The transcription factor COUP-TFII is negatively regulated by insulin and glucose via FoxO1 and ChREBP controlled pathways. . Mol Cell Biol 28: 6568-6579). Briefly, cells were transfected with COUP-TFII siRNA or a scrambled siRNA using a Amaxa device following manufacturer instructions.
Growth protocol The rat insulinoma 832/13 INS-1 cell line was used between passages 7 and 25. Cells were cultured at 5% CO2–95% air at 37°C in RPMI 640 medium containing 11 mM D-glucose supplemented with 10% (v/v) heat-inactivated fetal bovine serum, 100 U/ml penicillin-streptomycin, 10 mM HEPES, 1 mM sodium pyruvate (Invitrogen), and 50 μM β-mercaptoethanol (Invitrogen) (INS-1 medium).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted and purified from cultured cells using the RNA-Plus reagent according to the manufacturer’s instructions (Q-BIOgene).
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol starting from 1 ug total RNA (Expression Analysis Technical Manual, 701025 Rev5, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 ug of cRNA was hybridized for 16 hr at 45C on 230 2.0 rat Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the affymetrix 3000 genescanner
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was set to 150
 
Submission date Jul 08, 2011
Last update date Oct 07, 2011
Contact name Leentje Van Lommel
Organization name KULeuven
Department Molecular cell biology
Lab gene expression unit
Street address Herestraat 49 bus 901
City Leuven
ZIP/Postal code 3000
Country Belgium
 
Platform ID GPL1355
Series (1)
GSE30526 COUP-TFII Controls Mouse Postnatal Pancreatic β-Cell Mass through GLP-1 β-Catenin

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 108.741 P 0.000258358
AFFX-BioB-M_at 129.141 P 6.02111e-05
AFFX-BioB-3_at 63.1766 P 7.00668e-05
AFFX-BioC-5_at 89.3498 P 0.000126798
AFFX-BioC-3_at 84.7945 P 5.16732e-05
AFFX-BioDn-5_at 592.78 P 0.000126798
AFFX-BioDn-3_at 1334.46 P 0.000126798
AFFX-CreX-5_at 3982.24 P 5.16732e-05
AFFX-CreX-3_at 5863.01 P 4.42873e-05
AFFX-DapX-5_at 0.719695 A 0.749204
AFFX-DapX-M_at 8.93051 A 0.102165
AFFX-DapX-3_at 4.74741 A 0.672921
AFFX-LysX-5_at 0.533878 A 0.368416
AFFX-LysX-M_at 0.661089 A 0.804754
AFFX-LysX-3_at 3.29338 A 0.205712
AFFX-PheX-5_at 0.424681 A 0.973899
AFFX-PheX-M_at 0.398215 A 0.957038
AFFX-PheX-3_at 11.7547 A 0.165861
AFFX-ThrX-5_at 1.55581 A 0.916408
AFFX-ThrX-M_at 1.28181 A 0.659339

Total number of rows: 31099

Table truncated, full table size 950 Kbytes.




Supplementary file Size Download File type/resource
GSM756978_A22wt.CEL.gz 2.5 Mb (ftp)(http) CEL
GSM756978_A22wt.CHP.gz 168.8 Kb (ftp)(http) CHP
Processed data included within Sample table

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