|
Status |
Public on Mar 01, 2009 |
Title |
H1 hES cells |
Sample type |
RNA |
|
|
Source name |
H1 human ES cells
|
Organism |
Homo sapiens |
Characteristics |
H1 human ES cells
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated with Trizol.
|
Label |
Cy3
|
Label protocol |
Performed as described in One-Color Microarray-Based Gene Expression Analysis (Quick Amp Labeling) Protocol (Agilent, Version 5.7, March 2008).
|
|
|
Hybridization protocol |
Performed as described in One-Color Microarray-Based Gene Expression Analysis (Quick Amp Labeling) Protocol (Agilent, Version 5.7, March 2008).
|
Scan protocol |
Performed as described in One-Color Microarray-Based Gene Expression Analysis (Quick Amp Labeling) Protocol (Agilent, Version 5.7, March 2008).
|
Description |
Effect of p53 in iPS cell generation
|
Data processing |
Data were analyzed with GeneSpring GX 7.3.1. The parameters for normalization are as follows: Data transformation: Set measurement less than 0.01 to 0.01 Per chip: Normalize to 50th percentile
|
|
|
Submission date |
Oct 23, 2008 |
Last update date |
Oct 27, 2008 |
Contact name |
Shinya Yamanaka |
E-mail(s) |
yamanaka@cira.kyoto-u.ac.jp
|
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 |
GPL4133 |
Series (2) |
GSE13334 |
Effect of p53 in human iPS cell generation |
GSE13365 |
Effect of p53 on iPS cell generation |
|