|
Status |
Public on Aug 04, 2014 |
Title |
TIG108-4F3s19 |
Sample type |
RNA |
|
|
Source name |
human induced pluripotent stem cell line TIG108-4F3 subclone
|
Organism |
Homo sapiens |
Characteristics |
cell type: human induced pluripotent stem cell line TIG108-4F3 subclone
|
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
|
Description |
human induced pluripotent stem cell line TIG108-4F3 subclone
|
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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|
|
Submission date |
Feb 10, 2014 |
Last update date |
Aug 04, 2014 |
Contact name |
Kazutoshi Takahashi |
E-mail(s) |
kazu@cira.kyoto-u.ac.jp
|
Organization name |
Kyoto University
|
Department |
Center for iPS Cell Research and Application
|
Street address |
53 Kawahara-cho, Shogoin, Sakyo-ku
|
City |
Kyoto |
ZIP/Postal code |
606-8507 |
Country |
Japan |
|
|
Platform ID |
GPL14550 |
Series (1) |
GSE54848 |
Critical role of transient activation of human endogenous retroviruses during reprogramming toward pluripotency |
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