|
Status |
Public on Oct 03, 2006 |
Title |
hESC FGF2 re-stimulated exp1 |
Sample type |
RNA |
|
|
Source name |
cell line H9
|
Organism |
Homo sapiens |
Characteristics |
human embryonic stem cell line H9, passage 54
|
Treatment protocol |
hES cells were grown in MEF-conditioned medium on matrigel for 2 days, starved in unconditioned medium without FGF2 and with 30uM of SU5402 (Calbiochem), and, after extensive washing, re-treated with 40 ng/ml of FGF2 in UM for 4h, followed by RNA isolation.
|
Extracted molecule |
total RNA |
Extraction protocol |
Qiagen RNeasy kit with on-column DNA digestion following the manufacturer's instructions
|
Label |
Cy3
|
Label protocol |
Linear amplification kit Ambion #IL1791 following the manufacturer's instructions. Input amount: 300ng of total RNA; IVT: 6h
|
|
|
Hybridization protocol |
Employing materials and protocols by Illumina Inc.; hybridisation: 17h at 55 degC
|
Scan protocol |
Using an Illumina scanner; gain factor: 2.5
|
Description |
The control for this sample is hESC FGF2-starved exp1
|
Data processing |
In BeadStudio 1.0 raw data were background subtracted and normalised using the "rank invariant" algorithm. Value = "null" denotes expression below background (p < 0.01).
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|
|
Submission date |
Jul 31, 2006 |
Last update date |
Oct 03, 2006 |
Contact name |
Boris Greber |
E-mail(s) |
boris.greber@mpi-muenster.mpg.de
|
Organization name |
Max Planck Institute for Molecular Biomedicine
|
Department |
Cell and Developmental Biology
|
Street address |
Röntgenstraße 20
|
City |
Münster |
ZIP/Postal code |
48149 |
Country |
Germany |
|
|
Platform ID |
GPL2700 |
Series (1) |
GSE5415 |
hES cell FGF2 re-stimulation experiments |
|