|
| Status |
Public on Jun 27, 2006 |
| Title |
cRNA self-self hybridization 1 |
| Sample type |
RNA |
| |
|
| Channel 1 |
| Source name |
Ovary_epithelial_cell_line
|
| Organism |
Mus musculus |
| Characteristics |
in vitro amplified RNA, replica 1
|
| Extracted molecule |
total RNA |
| Label |
Cy3
|
| |
|
| Channel 2 |
| Source name |
Ovary_epithelial_cell_line
|
| Organism |
Mus musculus |
| Characteristics |
in vitro amplified RNA, replica1
|
| Extracted molecule |
total RNA |
| Label |
Cy5
|
| Label protocol |
Indirect labeling during in vitro amplification
|
| |
|
| |
| Hybridization protocol |
See Livesey, F. J., Furukawa, T., Steffen, M. A., Church, G. M. and Cepko, C. L. (2000). Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx. Curr Biol 10, 301-10
|
| Scan protocol |
Hybridised microarrays were scanned on a GenePix 4000B microarray scanner and the resulting images were analysed with GenePix 5 array analysis software
|
| Description |
RNA was extracted by the Invitrogen Trizol Protocol, Ref: Chomczynski, P. and Sacchi, N. (1987) Analytical Biochemistry 162, 156. 10 ug of total RNA was amplified in 3 rounds of T7-based amplification (MessageAmpII aRNA Kit, Ambion). cRNA was indirectly labeled with Cy3/Cy5 and co-hybridised on the slide
|
| Data processing |
Limma packadge: log-ratio were lowess normalized, filtered to exclude spots flagged as bad and backgroud corrected.
|
| |
|
| Submission date |
Jan 17, 2006 |
| Last update date |
Jun 27, 2006 |
| Contact name |
Tatiana Subkhankulova |
| E-mail(s) |
subkhankul@hotmail.com
|
| Phone |
02075941825
|
| Organization name |
Queen Mary University London
|
| Department |
Neuroscience
|
| Lab |
Silvia Marino
|
| Street address |
4 Newark Street
|
| City |
London |
| ZIP/Postal code |
E1 2AD |
| Country |
United Kingdom |
| |
|
| Platform ID |
GPL2584 |
| Series (1) |
| GSE5136 |
Comparison of linear and exponential amplification techniques for expression profiling at the single-cell level |
|
