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Status |
Public on May 16, 2015 |
Title |
TS_MIR replicate 2 |
Sample type |
RNA |
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|
Source name |
TS_MIR
|
Organism |
Mus musculus |
Characteristics |
age: adult tissue: hippocampus condition: trisomic transduction: Lv-miR155-802T
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNAs were prepared with Qiagen Rneasy minikit according to manufacturer’s protocol
|
Label |
Cy3
|
Label protocol |
100ng of total RNA from each sample were amplified by Oligo-dT-T7 reverse transcription and labeled by in vitro transcription with T7 RNA polymerase in the presence of Cy3-CTP using the LowInputQuick Amp Labeling kit (Agilent) and purified using RNAeasy columns (Qiagen, Hilden, Germany)
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Hybridization protocol |
After fragmentation, 600 ng of labeled cRNA from each sample was hybridized in in situ hybridization oven (Agilent) for 17 h at 65ºC and washed during 1 min at rt in Gene Expression Wash Buffer 1 (Agilent) and 1 min at 37 ºC with Gene Expression Wahs buffer 2 (Agilent).
|
Scan protocol |
Scanned on an Agilent G2539A scanner at 5um resolution and 100%PMT The intensity data of each individual hybridization were extracted and the quality was assessed with the Feature Extraction software 10.7 (Agilent).
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Data processing |
Raw data was corrected for background noise using the normexp method. Quantile normalization was applied to assure comparability across samples.
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Submission date |
Apr 20, 2015 |
Last update date |
May 16, 2015 |
Contact name |
Xavier Bofill-De Ros |
E-mail(s) |
xbofill@mbg.au.dk
|
Phone |
+13018465576
|
Organization name |
National Cancer Institute
|
Department |
RNA Biology Laboratory
|
Lab |
RNA mediated Gene Regulation
|
Street address |
1050 Boyles St., blg 560
|
City |
Frederick |
State/province |
MD |
ZIP/Postal code |
21702 |
Country |
USA |
|
|
Platform ID |
GPL13912 |
Series (1) |
GSE68074 |
Lentiviral vector-based microRNA sponges identifies miR-155 and miR-802 target genes in the hippocampus of Ts65Dn mice |
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