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Sample GSM1305975 Query DataSets for GSM1305975
Status Public on Jan 14, 2014
Title CF 5F SB Rep 2
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 11.558
10338002 7.73815
10338003 10.0137
10338004 8.6492
10338005 4.57386
10338006 4.84445
10338007 5.11775
10338008 5.56936
10338009 9.54032
10338010 4.62481
10338011 7.14975
10338012 4.74632
10338013 4.41678
10338014 4.48246
10338015 4.45373
10338016 8.97445
10338017 12.8904
10338018 8.11118
10338019 6.72703
10338020 9.48105

Total number of rows: 35556

Table truncated, full table size 586 Kbytes.




Supplementary file Size Download File type/resource
GSM1305975_4860_50105_CFS2_MoGene1.0st.CEL.gz 4.6 Mb (ftp)(http) CEL
GSM1305975_4860_50105_CFS2_MoGene1.0st.rma-gene-default.chp.gz 269.8 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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