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Sample GSM991853 Query DataSets for GSM991853
Status Public on Mar 31, 2013
Title rad53.MMS vs. rad53.UT, rep2
Sample type RNA
 
Channel 1
Source name rad53, untreated
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: rad53Δ
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 rad53, MMS
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: rad53Δ
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_251507211177_S01_H_flip_1-4.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 -0.310158429
A_06_P5727 0.000375163
A_06_P5667 0.195880952
A_06_P1931 -0.18138169
A_06_P2126 0.068305919
A_06_P5610 0.248596219
A_06_P3723 0.171459244
A_06_P1675 -0.138816863
A_06_P1087 -0.162436549
A_06_P6568 0.046993554
A_06_P7046 -0.177280408
A_06_P5705 -0.357871905
A_06_P3628 -0.263186591
A_06_P4724 -0.134190423
A_06_P6190 -0.318654251
A_06_P4910 -0.094331598
A_06_P2545 -0.022795489
A_06_P3168 0.320697739
A_06_P4543 0.095789448
A_06_P4487 0.355416973

Total number of rows: 6269

Table truncated, full table size 143 Kbytes.




Supplementary file Size Download File type/resource
GSM991853_US22502657_251507211177_S01_H_flip_1-4.avg.gpr.gz 443.5 Kb (ftp)(http) GPR
Processed data included within Sample table

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