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Sample GSM1366336 Query DataSets for GSM1366336
Status Public on Jun 04, 2014
Title shMsl1 ESC rep2_A
Sample type RNA
 
Source name ESC E14wt
Organism Mus musculus
Characteristics transduction: shMsl1 expression vector
background: 129P2/OlaHsd
Treatment protocol shRNA approaches were conducted with pLKO.1 puro shRNA vectors (Sigma-Aldrich, France) of the TRC2 library. For Ns1 KD the TRCN0000241466 shRNA clone and for Msl1 KD the TRCN0000241378 shRNA clone was used. In addition, the shRNA Non-Target Control (Product No. SHC002) was applied. Production of lentiviral particles as well as infection of mESCs was conducted according to the manufacturer’s protocol.
Growth protocol Wild type male mESCs (E14.wt) were cultivated on 0.1% gelatin and CD1 feeder cells (37°C, 5% CO2) in DMEM (4.5g/L), 15% foetal calf serum, leukemia inhibiting factor, penicillin/streptomycin, L-glutamine and non-essential amino acids. To work under feeder-free conditions cells were treated with 1mg/ml Collagenase (GIBCO) and 2mg/ml Dispase (GIBCO) and cultivated for one passage without feeder cells. Experiments were conducted at passage 26-29.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cDNA targets were prepared, starting from 150 ng of total RNA, using the Ambion WT Expression Kit (Cat 4411974) and the Affymetrix GeneChip WT Terminal Labeling Kit (Cat 900671) according to Affymetrix recommendations.
 
Hybridization protocol Following fragmentation and end-labeling, 3 ug of cDNAs were hybridized on GeneChip Mouse Gene 2.0 ST arrays (Affymetrix) for whole-transcript expression profiles.
Scan protocol Washed and stained chips were scanned with the GeneChip Scanner 3000 7G (Affymetrix) at a resolution of 0.7um.
Description Experiment A: gene expression data from shMsl1 ESCs
Data processing Obtained raw data (.CEL intensity files) were processed with Affymetrix Expression Console software version 1.1 to calculate probe set signal intensities using Robust Multi-array Average (RMA) algorithms with default settings.
 
Submission date Apr 09, 2014
Last update date Jun 05, 2014
Contact name Sarina Ravens
Organization name IGBMC
Street address 1 Rue Laurent Fries
City Illkirch
ZIP/Postal code 67404
Country France
 
Platform ID GPL16570
Series (1)
GSE56646 MOF-associated complexes have overlapping and unique roles in regulating pluripotency in embryonic stem cells and during differentiation [array]

Data table header descriptions
ID_REF
VALUE RMA

Data table
ID_REF VALUE
17210850 2.927662
17210852 3.202933
17210855 10.68039
17210869 10.38836
17210883 3.702228
17210887 9.0351
17210904 4.901961
17210912 9.223327
17210947 3.810493
17210953 4.193125
17210984 8.995919
17210994 3.590529
17210996 3.537275
17210998 3.43756
17211000 7.415484
17211004 5.728138
17211023 4.716817
17211033 4.544252
17211043 6.903656
17211066 3.948921

Total number of rows: 41345

Table truncated, full table size 722 Kbytes.




Supplementary file Size Download File type/resource
GSM1366336_DDS_shMsl1_ESC_rep2_A_MoGene2_2.CEL.gz 9.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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