|
| Status |
Public on Dec 19, 2007 |
| Title |
GL26 |
| Sample type |
RNA |
| |
|
| Channel 1 |
| Source name |
low grade brain tumor pool
|
| Organism |
Homo sapiens |
| Characteristics |
pool of 4 oligodendrogliomas(OL), 5 pilocytic astrocytomas (PA), 2 fibrillary astrocytomas (FA)
|
| Biomaterial provider |
Luca Morandi
|
| Treatment protocol |
Fresh frozen biopsies in liquid nitrogen and put them at -80. After thawing, RNA Later treatment before tissue homogenization.
Total RNA was measured by Bioanalyzer 2100 (Agilent): 28S/18S ratio= 1.66
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Protect RNAeasy Mini kit protocol (Qiagen)
|
| Label |
Cy3
|
| Label protocol |
The labeled cRNA was generated by in vitro transcription with the use of T7
RNA polymerase (low RNA input fluorescent linear amplification kit
Agilent cod. 5184-3523).
|
| |
|
| Channel 2 |
| Source name |
GL26
|
| Organism |
Homo sapiens |
| Characteristics |
Fresh frozen biopsy from right frontal glioblastoma of a 34 years old women. Overall Survival (months): 10.1
|
| Biomaterial provider |
Luca Morandi
|
| Treatment protocol |
Fresh frozen in liquid nitrogen and put at -80. After thawing, RNA Later treatment before tissue homogenization.
Total RNA was measured by Bioanalyzer 2100 (Agilent): 28S/18S ratio=1.54
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Protect RNAeasy Mini kit protocol (Qiagen)
|
| Label |
Cy5
|
| Label protocol |
The labeled cRNA was generated by in vitro transcription with the use of T7
RNA polymerase (low RNA input fluorescent linear amplification kit
Agilent cod. 5184-3523).
|
| |
|
| |
| Hybridization protocol |
0.75 ug of labeled test and reference cRNA were fragmented and hybridized at 60 C for 17 hours.
The washing steps were done following the SSC protocol (version 3.0, Agilent)
|
| Scan protocol |
After hybridization and washes, the slides were scanned with a confocal laser scanner (Agilent G2565BA).
|
| Description |
Fluorescent
intensities on scanned images were quantified by the feature extraction
software 7.5, and LogRatio data were available for further statistical
analysis.
|
| Data processing |
The
scan data were analysed with Agilent Feature Extraction Software, which
performs spots localization (Find Spot Algorhythm), outlier pixels
rejection based on the Interquartile Range method (Cookie Cutter
Algorhythm), flagging of saturated features (a feature is considered
saturated when more than 50% of its pixels had an intensity above
65502). Loess normalization and between array scale normalization were
performed using the “LIMMA” package of Bioconductor
(www.bioconductor.org).
|
| |
|
| Submission date |
Dec 13, 2007 |
| Last update date |
Aug 14, 2011 |
| Contact name |
Luca Morandi |
| E-mail(s) |
[email protected]
|
| Organization name |
University of Bologna
|
| Department |
Oncology Dept
|
| Lab |
Anatomia Patologica Bellaria Hospital
|
| Street address |
Via Altura 3
|
| City |
Bologna |
| ZIP/Postal code |
40139 |
| Country |
Italy |
| |
|
| Platform ID |
GPL885 |
| Series (1) |
| GSE9885 |
Gene expression profiling in glioblastoma and immunohistochemical evaluation of IGFBP-2 and CDC20 |
|
