|
Status |
Public on May 13, 2009 |
Title |
Cardiac Progenitor WT2 |
Sample type |
RNA |
|
|
Source name |
Embryonic Cardiac Progenitors - wild type
|
Organism |
Mus musculus |
Characteristics |
cell type: E9.0 embryonic cardiac progenitors
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction
|
Label |
Biotin
|
Label protocol |
Total RNA was amplified with the WT-Ovation Pico RNA Amplification System, fragmented and labeled with the FL-Ovation cDNA Biotin Module V2 (Nugen).
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|
|
Hybridization protocol |
Performed as manufacturer's protocol (Affymetrics)
|
Scan protocol |
Performed as manufacturer's protocol (Affymetrics)
|
Description |
YFP+ cells marking precardiac mesoderm were FACS-sorted (w/wo stabilized Beta-catenin), and their total RNA was isolated, amplified and labeled with the NUGENE pico kit for microarray analyses. Mutant samples were obtained from YFP+ cells isolated from embryos with Isl1-cre, Rosa-YFP, Beta-catenin (loxP ex3). The mutants are conditional knockout mouse embryos that activates stable Beta-catenin in cardiac progenitors.
|
Data processing |
Raw data generated from at least three independent experiments were further analyzed by the group of Dr. Ru-Fang Yeh at the Center for Informatics and Molecular Biostatistics, UCSF.
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|
|
Submission date |
Mar 13, 2009 |
Last update date |
Mar 16, 2009 |
Contact name |
Chulan Kwon |
E-mail(s) |
[email protected]
|
Organization name |
Gladstone Institutes
|
Street address |
1650 Owens Street
|
City |
San Francisco |
State/province |
CA |
ZIP/Postal code |
94158 |
Country |
USA |
|
|
Platform ID |
GPL1261 |
Series (1) |
GSE15232 |
A Regulatory Pathway Involving Notch1/β-Catenin/Isl1 Determines Cardiac Progenitor Cell Fate |
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