|
Status |
Public on Oct 01, 2008 |
Title |
oxidative stress, t=0 |
Sample type |
RNA |
|
|
Source name |
time 0 following H2O2 treatment
|
Organism |
Saccharomyces cerevisiae |
Characteristics |
strain Y262
|
Treatment protocol |
At time 0, cells were treated with 0.3mM of H2O2 or 0.1% of MMS.
|
Growth protocol |
Cells were grown in YPD to mid-log phase in 25 degrees.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using MasterPureā¢ (EPICENTER Biotechnologies).
|
Label |
biotin
|
Label protocol |
cDNA was prepared using poly(T) primers, labeled cRNA was prepared using the GeneChip system according to manufacturer instructions.
|
|
|
Hybridization protocol |
GeneChip system according to manufacturer instructions.
|
Scan protocol |
GeneChip system according to manufacturer instructions.
|
Description |
Gene expression following treatment with 0.3mM of H2O2
|
Data processing |
RMA algorithms using bioconductor software implemented in R.
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|
|
Submission date |
Jul 23, 2008 |
Last update date |
Jul 24, 2008 |
Contact name |
Ophir Shalem |
E-mail(s) |
[email protected]
|
Organization name |
Weizmann Inst.
|
Street address |
Hertzel
|
City |
Rehovot |
ZIP/Postal code |
76100 |
Country |
Israel |
|
|
Platform ID |
GPL2529 |
Series (2) |
GSE12220 |
Changes in Saccharomyces cerevisiae mRNA abundance following oxidative stress and DNA damage stress |
GSE12222 |
Transient transcriptional responses to stress are generated by opposing effects of mRNA production and degradation |
|