|
Status |
Public on Jan 01, 2013 |
Title |
undifferentiated Sox17-GFP mES cells |
Sample type |
RNA |
|
|
Source name |
Sox17-GFP mESC_undifferentiated
|
Organism |
Mus musculus |
Characteristics |
strain background: 129 genotype/variation: Sox17-GFP cell type: mESC
|
Treatment protocol |
Endoderm differentiation was induced for 6-8 days in DMEM, 5% FBS, 0.1mM NEAA, 1x Glutamax, 1x Penn/Strep, 0.055mM βMe, supplemented with 50 ng/ml recombinant human Activin A or 1000ng/ml recombinant mouse Nodal; media changed every other day.
|
Growth protocol |
Mouse ES cells were maintained on gelatin-coated plates with MEFs in DMEM, 0.1mM NEAA, 1x Glutamax, 1x Penn/Strep (Invitrogen), 15% FBS (HyClone), 0.055mM 2-mercaptoethanol (βMe; Sigma), and 5x10^5 units LIF (Chemicon)
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA isolated using Qiashredder and RNAeasy Mini Kit. Biotinylated cRNA prepared from ≥100ng of RNA using Illumina TotalPrep RNA Amplification Kit.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
|
|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
4 replicates for each sample
|
Data processing |
The data were normalized using cubic spline with Bead Studio v2.0
|
|
|
Submission date |
Sep 22, 2012 |
Last update date |
Jan 01, 2013 |
Contact name |
Alice E Chen |
Organization name |
Harvard University
|
Department |
Stem Cell and Regenerative Biology
|
Lab |
Douglas Melton
|
Street address |
7 Divinity Avenue
|
City |
Cambridge |
State/province |
Ma |
ZIP/Postal code |
02138 |
Country |
USA |
|
|
Platform ID |
GPL6885 |
Series (1) |
GSE41086 |
Gene expression profiling of Nodal versus Activin-derived endoderm from mouse ES cells |
|