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Status |
Public on Nov 22, 2012 |
Title |
ES cells GFP shRNA rep1-rep4 |
Sample type |
RNA |
|
|
Source name |
ES cells GFP shRNA
|
Organism |
Mus musculus |
Characteristics |
dev stage: E14 cell type: Embryonic Stem Cells
|
Treatment protocol |
shRNAs for GFP, Esrrb and Sox2 were transfected into mouse ES cells using lipofecatmine. Transfectants were slected by puromycin for 2 days and RNA harvested for microarray analysis
|
Growth protocol |
normal ES cell conditions
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with TRIzol reagent, followed by purification using the QIAGEN RNeasy mini kit according to the manufacturers protocol. Quality control was performed with Agilent Bioanalyser.
|
Label |
biotin
|
Label protocol |
Standard Illumina Protocol
|
|
|
Hybridization protocol |
Standard Illumina Protocol
|
Scan protocol |
Standard Illumina Protocol
|
Data processing |
The data was normalised using GeneSpring 7. Merged 4 biological replicates to give a mean (transformed) expression and stdev value.
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|
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Submission date |
Dec 05, 2011 |
Last update date |
Nov 22, 2012 |
Contact name |
Andrew P Hutchins |
E-mail(s) |
[email protected]
|
Organization name |
Southern University of Science and Technology
|
Department |
Bioinformatics
|
Lab |
Bioinformatics and Genomics
|
Street address |
1088 Xueyuan Rd
|
City |
Shenzhen |
ZIP/Postal code |
518055 |
Country |
China |
|
|
Platform ID |
GPL6885 |
Series (1) |
GSE34170 |
Dual knockdown of Esrrb and Sox2 in mouse embryonic stem cells |
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