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Sample GSM2466750 Query DataSets for GSM2466750
Status Public on Sep 04, 2017
Title siCBP_HPM_T72 diff
Sample type RNA
 
Source name HPM transfected with siCBP at time 72h
Organism Homo sapiens
Characteristics time: 72h of differentiation
cell type: Primary myoblasts
patient id: M38
Treatment protocol Human Primary Myoblasts (HPM) were grown to confluence, transfectedor not with siRNA (either control, or CBP or CBP or CBP+p300) and induced 24h later for differentiation by decreasing serum concentration.
Growth protocol myoblasts were plated in Petri dishes and cultured in growth medium containing Dulbecco’s Modified Eagle’s Medium (Gibco) supplemented with 20% fetal bovine serum (GE Healthcare, PAA) 1% Ultroser G serum substitute (PALL life sciences) and 50μg/ml Gentamicin (Thermo Scientific) at 37°C in humidified atmosphere with 5% CO2. All experiments were carried out between P4 and P8 to avoid cell senescence. Myogenic differentiation of confluent cells was induced by changing growth medium to DMEM containing 2% FBS and 50μg/ml Gentamicin (differentiation medium).
Extracted molecule total RNA
Extraction protocol Total RNAs were extracted from cells using Aurum Total RNA Mini Kit (Bio-rad) according to manufacturer’s instructions
Label biotin
Label protocol Biotinylated single strand cDNA targets were prepared, starting from 150 ng of total RNA, using the Ambion WT Expression Kit and the Affymetrix GeneChip® WT Terminal Labeling Kit according to Affymetrix recommendations
 
Hybridization protocol Following fragmentation and end-labeling, 3 μg of cDNAs were hybridized for 16 h at 45oC on GeneChip® Human Gene 2.0 ST arrays (Affymetrix)
Scan protocol The chips were washed and stained in the GeneChip® Fluidics Station 450 (Affymetrix) and scanned with the GeneChip® Scanner 3000 7G (Affymetrix) at a resolution of 0.7 µm
Data processing Raw data (.CEL Intensity files) were extracted from the scanned images using the Affymetrix GeneChip® Command Console (AGCC) version 3.2.
CEL files were further processed with Affymetrix Expression Console software version 1.3.1 to calculate probe set signal intensities using Robust Multi-array Average (RMA) algorithms with default setings
 
Submission date Jan 24, 2017
Last update date Sep 04, 2017
Contact name Laurence Vandel
E-mail(s) laurence.vandel@univ-tlse3.fr
Organization name CNRS
Department CBD
Street address 118 ROute de Narbonne
City Toulouse
ZIP/Postal code 31062
Country France
 
Platform ID GPL16686
Series (1)
GSE94006 Analysis of the common and respective roles of CBP and p300 co-activators in human primary myoblast differentiation.

Data table header descriptions
ID_REF
VALUE RMA

Data table
ID_REF VALUE
16657436 7.385161
16657440 5.809237
16657445 3.397796
16657447 3.088937
16657450 9.124573
16657469 7.120781
16657473 3.367615
16657476 6.566895
16657480 4.663306
16657485 2.714962
16657489 5.039493
16657492 4.988853
16657502 6.540267
16657506 4.892099
16657509 4.18546
16657514 7.356362
16657527 5.203358
16657529 5.39389
16657534 5.82667
16657554 6.650652

Total number of rows: 53617

Table truncated, full table size 936 Kbytes.




Supplementary file Size Download File type/resource
GSM2466750_HGR_CB-72_HuGene2.CEL.gz 8.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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