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Sample GSM1305967 Query DataSets for GSM1305967
Status Public on Jan 14, 2014
Title MEF 5F SB Rep 3
Sample type RNA
 
Source name MEFs treated with 5F in the presence of 0.5 uM SB
Organism Mus musculus
Characteristics cell type: embryonic fibroblast
treatment: 5F in the presence of 0.5 uM SB
Treatment protocol MEFs were plated into poly-L-lysine-coated 6 well dishes at 75,000 cells/well on Day -2, with 500 μL (≥ 2.5x105 IFU) each of rtTA lentivirus (FUdeltaGW-rtTA, Addgene plasmid 19780) and TroponinT-GCaMP-Zeo reporter lentivirus per well with 2 mL MEF medium. The following day (Day -1), culture medium was replaced with 2 mL fresh MEF medium with the molecules or DMSO vehicle and cells were transduced with 500 μL (≥ 2.5x105 IFU) of each tetO-transcription factor lentivirus. The next day (Day 0), medium was switched to 3 mL/well Reprogramming Medium consisting of AGM (Lonza CC-3186) without EGF, supplemented with 2 μg/mL doxycycline (Sigma).
Growth protocol MEFs were grown in DMEM with 10% fetal bovine serum and 1X Glutamax.
Extracted molecule total RNA
Extraction protocol Cells were collected in Trizol at Day 3 post-transduction. Non-transduced MEFs were cultured and collected at Day 3. Samples were collected in triplicate from independent biological replicates and total RNA was prepared by the University of Pennsylvania Molecular Profiling Facility.
Label biotin
Label protocol The labeling, hybridization, and scanning procedures were performed by the University of Pennsylvania Molecular Profiling facility
 
Hybridization protocol The labeling, hybridization, and scanning procedures were performed by the University of Pennsylvania Molecular Profiling facility
Scan protocol The labeling, hybridization, and scanning procedures were performed by the University of Pennsylvania Molecular Profiling facility
Description MEF 5TF treatment SB
Gene expression data from SB treated MEFs that received 5TF treatment
Data processing Initial data analysis was performed using Affymetrix Microarray Suite 5.0 and further analyzed using PartekGS software.
 
Submission date Jan 13, 2014
Last update date Jan 14, 2014
Contact name John Gearhart
E-mail(s) gearhart@upenn.edu
Phone 215-898-4450
Organization name University of Pennsylvania
Department Dept of Cell and Developmental Biology, Institute for Regenerative Medicine
Street address 3400 Civic Center Blvd, Building 421, 9-121 Smilow Center for Translational Research
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platform ID GPL6246
Series (1)
GSE54022 Inhibition of TGFβ Signaling Increases Direct Conversion of Fibroblasts to Induced Cardiomyocytes

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
10338001 12.2526
10338002 8.17079
10338003 10.8417
10338004 9.43621
10338005 5.01514
10338006 5.25141
10338007 5.50975
10338008 5.98479
10338009 9.91491
10338010 5.07997
10338011 7.53141
10338012 5.1319
10338013 4.87189
10338014 4.92629
10338015 4.91135
10338016 9.42214
10338017 13.2849
10338018 8.62335
10338019 7.10716
10338020 9.84177

Total number of rows: 35556

Table truncated, full table size 586 Kbytes.




Supplementary file Size Download File type/resource
GSM1305967_4766_48459_5FS3_MoGene1.0st.CEL.gz 4.6 Mb (ftp)(http) CEL
GSM1305967_4766_48459_5FS3_MoGene1.0st.rma-gene-default.chp.gz 270.5 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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