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Status |
Public on Dec 03, 2013 |
Title |
246G1(p23)_undiff.hiPS_SFEBq_good |
Sample type |
RNA |
|
|
Source name |
undifferentiated hiPS
|
Organism |
Homo sapiens |
Characteristics |
cell type: undiff_hiPS method: Retrovirus cell origin: BJ transduction: OSKM sfebq: differentiation good
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated by Trizol reagent (Life Technologies) according to the manufacturer's instruction.
|
Label |
Cy3
|
Label protocol |
Agilent standard protocol
|
|
|
Hybridization protocol |
Agilent standard protocol
|
Scan protocol |
Agilent standard protocol
|
Data processing |
The data were analyzed using the Gene Spring GX 11.5.1 software program (Agilent Technologies).The data processing was performed as follows; (i) Threshold raw signals were set to 1.0, (ii) Log base 2 transformation was performed, (iii) 75th percentile normalization was chosen as the normalized algorithm.
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|
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Submission date |
Nov 21, 2012 |
Last update date |
Dec 03, 2013 |
Contact name |
Shinya Yamanaka |
E-mail(s) |
[email protected]
|
Phone |
81-75-366-7041
|
Organization name |
Center for iPS Cell Research and Applicaton (CiRA), Kyoto University
|
Street address |
53 Kawahara-machi, Shogoin, Sakyo-ku
|
City |
Kyoto |
ZIP/Postal code |
606-8507 |
Country |
Japan |
|
|
Platform ID |
GPL14550 |
Series (2) |
GSE42452 |
Comparison of gene expression profilings between SFEBq differentiation-defective clones and good clones |
GSE49053 |
Differentiation defective phenotypes revealed by large scale analyses of human pluripotent stem cells |
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