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Sample GSM991817 Query DataSets for GSM991817
Status Public on Mar 31, 2013
Title ste11.MMS vs. ste11.UT, rep1
Sample type RNA
 
Channel 1
Source name ste11, untreated
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: ste11Δ
treatment: none
Treatment protocol Conditions are untreated (UT) or methyl methanesulfonate (MMS-0.033%) treated.
Growth protocol For these experiments, 100 ml cultures for each strain were grown to an OD600 density of 0.8-1.0 at 30oC, split into two 50 ml cultures, and incubated for one additional hour either in the presence (MMS-treated) or absence (untreated) of 0.03% MMS (methyl methanesulfonate; Sigma 129925).
Extracted molecule total RNA
Extraction protocol RNA was isolated by hot phenol/chloroform extraction and enriched for mRNA via the Poly(A) Purist Kit (Ambion AM1916, Austin, TX, USA).
Label Cy3
Label protocol As described in Kuo D, Tan K, Zinman G, Ravasi T, Bar-Joseph Z, Ideker T (2010) Evolutionary divergence in the fungal response to fluconazole revealed by soft clustering. Genome Biol 11: R77 (PMID 20653936).
 
Channel 2
Source name ste11, MMS
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: ste11Δ
treatment: methyl methanesulfonate (MMS)
Treatment protocol Conditions are untreated (UT) or methyl methanesulfonate (MMS-0.033%) treated.
Growth protocol For these experiments, 100 ml cultures for each strain were grown to an OD600 density of 0.8-1.0 at 30oC, split into two 50 ml cultures, and incubated for one additional hour either in the presence (MMS-treated) or absence (untreated) of 0.03% MMS (methyl methanesulfonate; Sigma 129925).
Extracted molecule total RNA
Extraction protocol RNA was isolated by hot phenol/chloroform extraction and enriched for mRNA via the Poly(A) Purist Kit (Ambion AM1916, Austin, TX, USA).
Label Cy5
Label protocol As described in Kuo D, Tan K, Zinman G, Ravasi T, Bar-Joseph Z, Ideker T (2010) Evolutionary divergence in the fungal response to fluconazole revealed by soft clustering. Genome Biol 11: R77 (PMID 20653936).
 
 
Hybridization protocol According to the protocol recommended by Agilent.
Scan protocol GenePix 4000A Scanner, Quantitation w/ GenePix 6.0.
Description US22502657_251507211009_S01_H_flip_4-4.avg
Data processing Lowess normalized, quantile normalized, LIMMA model.
 
Submission date Aug 23, 2012
Last update date May 07, 2013
Contact name Eric Jaehnig
E-mail(s) ejaehnig@ucsd.edu
Organization name Ludwig Institute for Cancer Research
Department Laboratory of Cancer Genetics
Lab Kolodner
Street address 9500 Gilman Dr
City La Jolla
State/province CA
ZIP/Postal code 92093
Country USA
 
Platform ID GPL9294
Series (1)
GSE40351 DNA damage checkpoint kinases regulate a global network of transcription factors

Data table header descriptions
ID_REF
VALUE Lowess- and quantile-normalized log2 ratio (MMS/UT)

Data table
ID_REF VALUE
A_06_P1519 -0.622012875
A_06_P5727 0.022208536
A_06_P5667 0.018602158
A_06_P1931 0.594695328
A_06_P2126 -0.120943392
A_06_P5610 1.343549291
A_06_P3723 0.701851223
A_06_P1675 0.112649004
A_06_P1087 -0.054242298
A_06_P6568 -0.441725879
A_06_P7046 0.326887808
A_06_P5705 -0.894552795
A_06_P3628 -0.134792118
A_06_P4724 -0.064305996
A_06_P6190 0.416277802
A_06_P4910 -0.374538265
A_06_P2545 -0.27179277
A_06_P3168 0.175286589
A_06_P4543 -0.039720475
A_06_P4487 0.343960658

Total number of rows: 6269

Table truncated, full table size 143 Kbytes.




Supplementary file Size Download File type/resource
GSM991817_US22502657_251507211009_S01_H_flip_4-4.avg.gpr.gz 818.3 Kb (ftp)(http) GPR
Processed data included within Sample table

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