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Status |
Public on Oct 01, 2009 |
Title |
p4_rep1 |
Sample type |
RNA |
|
|
Source name |
Embryonic stem cells, fraction p4
|
Organism |
Homo sapiens |
Characteristics |
HES2 standard culture
|
Treatment protocol |
HES2 cells were subjected to FACs sorting, and fractions p4, p5, p6, and p7 were collected.
|
Growth protocol |
HES2 ESCs were grown in standard ES culture conditions.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA samples were prepared using Qiagen RNeasy Micro Kit (Qiagen) and then assayed using the Agilent Systems Bioanalyzer 2100 to ensure that high-quality RNA was used for the array experiments.
|
Label |
Cy3
|
Label protocol |
Targets were prepared from 100 ng total RNA using the Illumina TotalPrep RNA Amplification Kit (Ambion, catalog #AMIL1791).
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|
|
Hybridization protocol |
Illumina Human 6 BeadChips were hybridized, washed, stained and scanned according to Illumina's protocol.
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Scan protocol |
Processed arrays were read using Illumina BeadReader according to the manufacturer's instructions.
|
Description |
Replicate 1 of 3 1705168044_A
|
Data processing |
Data were first extracted with Illumina BeadStudio software without normalisation. Data was then uploaded into R, where RMA background adjustment and Quantile normalisation was performed using the BeadExplorer package.
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Submission date |
Oct 14, 2008 |
Last update date |
Oct 01, 2009 |
Contact name |
Sean Grimmond |
E-mail(s) |
[email protected]
|
Organization name |
University of Queensland
|
Department |
Institute for Molecular Bioscience
|
Lab |
Expression Genomics Lab
|
Street address |
Services Rd
|
City |
St Lucia |
State/province |
Q |
ZIP/Postal code |
4072 |
Country |
Australia |
|
|
Platform ID |
GPL6102 |
Series (1) |
GSE13201 |
HES2 embryonic stem cells (ESCs) grown in standard conditions and FACs sorted for GCTM-2 and CD9 |
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