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Sample GSM1305974 Query DataSets for GSM1305974
Status Public on Jan 14, 2014
Title CF 5F SB Rep 1
Sample type RNA
 
Source name CFs treated with 5F in the presence of 5 uM SB
Organism Mus musculus
Characteristics cell type: cardiac fibroblast
treatment: 5F in the presence of 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 CF 5TF treatment SB
Gene expression data from SB treated CFs 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 11.5716
10338002 7.87762
10338003 10.0829
10338004 8.63313
10338005 4.56295
10338006 4.83948
10338007 5.13521
10338008 5.62652
10338009 9.74874
10338010 4.60759
10338011 7.26041
10338012 4.71732
10338013 4.40291
10338014 4.47334
10338015 4.4444
10338016 9.1249
10338017 12.7845
10338018 8.25808
10338019 6.81472
10338020 9.66031

Total number of rows: 35556

Table truncated, full table size 586 Kbytes.




Supplementary file Size Download File type/resource
GSM1305974_4860_50104_CFS1_MoGene1.0st.CEL.gz 4.5 Mb (ftp)(http) CEL
GSM1305974_4860_50104_CFS1_MoGene1.0st.rma-gene-default.chp.gz 269.6 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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