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Status |
Public on May 31, 2006 |
Title |
d5 empty vector MOE430A |
Sample type |
RNA |
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Source name |
ES cells (CCE cell line) d5 empty vector
|
Organism |
Mus musculus |
Characteristics |
Mouse embrionic stem cells Gender: male Strain: 129/Sv
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Treatment protocol |
48 hours after transduction cells were re-plated at the density 0.3x10^6 cells per 10 cm dish. Simultaneously, GFP+ cells were FACS purified and used as day 0 time point. Re-plated cells were maintained in the presence of LIF. GFP+ cells from each culture were FACS purified every day for 7 consecutive days to obtain 8 day time course (d0-d7).
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Growth protocol |
Cells were maintained in the presence of LIF 1000 unit/ml.
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Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA probes were synthesized using the BioArray High-Yield Transcript Labeling Kit (Enzo Diagnostics, Farmingdale, NY).
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Hybridization protocol |
15 micrograms of biotin-labeled cRNA was fragmented for 35min. at 94C in fragmentation buffer (Affymetrix; Santa Clara, CA), and hybridized to Affymetrix MOE 430 A and B oligonucleotide microarrays.
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Scan protocol |
GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
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Description |
Gene expression data from ES cells transduced with empty vector at d5.
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Data processing |
The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method.
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Submission date |
Apr 17, 2006 |
Last update date |
Apr 18, 2006 |
Contact name |
Ihor Lemischka |
Organization name |
Princeton University
|
Street address |
Washington Rd
|
City |
Princeton |
State/province |
NJ |
ZIP/Postal code |
08540 |
Country |
USA |
|
|
Platform ID |
GPL339 |
Series (1) |
GSE4679 |
shRNAi induced differentiation time courses in mouse embrionic stem cells. |
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