|
Status |
Public on Aug 02, 2014 |
Title |
Group C_Experiment_30 days_rep4 |
Sample type |
RNA |
|
|
Source name |
primary lung adenocarcinoma
|
Organism |
Mus musculus |
Characteristics |
strain: Lox-stop-lox Kras G12D mice infected with: adenovirus CRE (Ad-Cre) tissue: lung tissue type: primary lung adenocarcinoma cell type: Sca-1+CD34+ cells
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA are harvested using TRIzol (Invitrogen) and RNeasy mini kit (QIAGEN) according to manufacturer’s instructions.
|
Label |
Hy3
|
Label protocol |
After having passed RNA measurement on the Nanodrop instrument, the samples are labeled using the miRCURY™ Hy3™/Hy5™ Power labeling kit and hybridized on the miRCURY™ LNA Array (v.11.0).
|
|
|
Hybridization protocol |
The samples were hybridized on a hybridization station following the scheme you outlined in the sample submission.
|
Scan protocol |
Scanning is performed with the Axon GenePix 4000B microarray scanner. GenePix pro V6.0 is used to read the raw intensity of the image.
|
Data processing |
The intensity of green signal is calculated after background subtraction and replicated spots on the same slide have been averaged by getting a median intensity. We use Median Normalization Method to obtain “Normalized Data”, Normalized Data=(Foreground-Background)/median, the median is 50 percent quantile of microRNA intensity which is larger than 50 in all samples after background correction.
|
|
|
Submission date |
Aug 01, 2014 |
Last update date |
Aug 02, 2014 |
Contact name |
guo zhen zhao |
E-mail(s) |
zlpjyo@126.com
|
Organization name |
Cancer Institute of PLA, Xinqiao Hospital, Third Military Medical University,
|
Street address |
Cancer Institute of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, China
|
City |
chongqing |
ZIP/Postal code |
400037 |
Country |
China |
|
|
Platform ID |
GPL19029 |
Series (1) |
GSE60001 |
MicroRNA profile of tumorigenic cells during formation of pulmonary adenocarcinoma |
|