|
Status |
Public on Dec 03, 2013 |
Title |
DP74_soma |
Sample type |
RNA |
|
|
Source name |
Dental Pulp cells
|
Organism |
Homo sapiens |
Characteristics |
cell type: soma
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated by Trizol reagent (Life Technologies) according to the manufacturer's instruction.
|
Label |
biotin
|
Label protocol |
Samples were enzymatically fragmented and biotinylated using the WT Terminal labeling Kit (Affymetrix).
|
|
|
Hybridization protocol |
Approximately 5.5ug of labeled DNA target was hybridized to the Affymetrix GeneChip Human Exon 1.0 ST Array at 45℃ for 17 hrs according to the manufacturer's recommendation.
|
Scan protocol |
Hybridized arrays were washed and satined on a GeneChip Fluidics Satation 450 and scanned on a GCS3000 Scanner (Affymetrix).
|
Data processing |
The exon array data analysis was performed using the Gene Spring GX11.5.1 software. Summarization algorithme:ExonPLIER16 with core and extended probe sets. probe group file: HuEx-1_0-st-v2_na32_hg19_2011-06-23
|
|
|
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 |
GPL5175 |
Series (2) |
GSE42449 |
Exon array analysis for SFEBq differentiation-defective clones and good clones |
GSE49053 |
Differentiation defective phenotypes revealed by large scale analyses of human pluripotent stem cells |
|