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Status |
Public on Apr 11, 2011 |
Title |
breast tissue, Neg Contr., Rep. 5 |
Sample type |
RNA |
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Source name |
breast tissue of WAP-TNP8 mice bevor activation of the SV40 oncogene
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Organism |
Mus musculus |
Characteristics |
strain: WAP-TNP8 tissue: breast
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Treatment protocol |
Breast tissue was snap frozen directly after preparation and stores at -80°C until RNA isolation.
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Growth protocol |
WAP-TNP8 animals, which selectively synthesize the T/t-antigen under the control of the WAP promoter in mammary gland epithelial cells, were used for this study (Schulze-Garg et al. 2000)
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Extracted molecule |
total RNA |
Extraction protocol |
Rneasy Kit (Qiagen) was used according to the manufacturer's instructions.
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Label |
biotin
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Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 50 ng total RNA (GeneChip® Two-Cycle Target Labelling Kit (Affymetrix)).
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Hybridization protocol |
Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45°C on GeneChip Human Genome U133 Plus 2.0 Array.
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Scan protocol |
GeneChips were scanned using the GeneChip Scanner 3000 (Affymetrix).
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Data processing |
GeneSpring GX 10.0 (Agilent) was used for data analysis.
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Submission date |
Apr 21, 2010 |
Last update date |
Apr 11, 2011 |
Contact name |
Celine Schäfer |
E-mail(s) |
celine.schaefer@charite.de
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Organization name |
Charité
|
Department |
Med. Kl. m.S. Hepatologie und Gastroenterologie
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Lab |
AG Grötzinger
|
Street address |
Augustenburger Platz 1
|
City |
Berlin |
ZIP/Postal code |
13353 |
Country |
Germany |
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Platform ID |
GPL1261 |
Series (1) |
GSE21444 |
Expression profiling of murine DCIS and invasive ductal breast carcinoma |
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