|
Status |
Public on Nov 20, 2012 |
Title |
FL2 CNTRL siRNA untreated repeat 1 |
Sample type |
RNA |
|
|
Source name |
FL2 CNTRL siRNA untreated repeat 1
|
Organism |
Homo sapiens |
Characteristics |
cell type: normal diploid human fetal lung fibroblast transfection: FL2 CNTRL siRNA
|
Treatment protocol |
Exponentially growing cells treated with 200ng/mL doxorubicin or sham for 26 hours.
|
Growth protocol |
Cells were propogated according to standard cell culture conditions for indicated cell lines.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was isolated by Trizol extraction and Qiagen RNAeasy spin column. DNA contamination eliminated by DNAse treatment. RNA quality was evaluated by Agilent Bioanalyser.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
|
|
|
Hybridization protocol |
Standard illumina hybridization protocol.
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
biological replicate 1
|
Data processing |
The data were normalised using quantile normalisation with IlluminaGUI in R
|
|
|
Submission date |
Nov 19, 2012 |
Last update date |
Sep 13, 2016 |
Contact name |
Adam Schmitt |
E-mail(s) |
amschmit@stanford.edu
|
Phone |
650-736-0305
|
Fax |
650-723-8762
|
Organization name |
Stanford University
|
Department |
Department of Dermatology
|
Lab |
Howard Y. Chang
|
Street address |
269 Campus Drive
|
City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305-5168 |
Country |
USA |
|
|
Platform ID |
GPL6947 |
Series (2) |
GSE42368 |
p53-dependent regulation of gene expression following DNA damage |
GSE76420 |
LncRNA DINO guides DNA damage signaling |
|