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Sample GSM991821 Query DataSets for GSM991821
Status Public on Mar 31, 2013
Title chk1.MMS vs. chk1.UT, rep1
Sample type RNA
 
Channel 1
Source name chk1, untreated
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: chk1Δ
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 chk1, MMS
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: chk1Δ
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_251507211010_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 -0.423490538
A_06_P5727 0.11759255
A_06_P5667 -0.194736046
A_06_P1931 0.723741815
A_06_P2126 0.108700569
A_06_P5610 1.260116955
A_06_P3723 0.257404199
A_06_P1675 -0.001965574
A_06_P1087 0.11072872
A_06_P6568 -0.310582164
A_06_P7046 0.062677666
A_06_P5705 -0.544530836
A_06_P3628 -0.552705844
A_06_P4724 -0.065177999
A_06_P6190 0.491876025
A_06_P4910 -0.274437935
A_06_P2545 -0.326770891
A_06_P3168 0.495878668
A_06_P4543 -0.205915818
A_06_P4487 0.128660645

Total number of rows: 6269

Table truncated, full table size 143 Kbytes.




Supplementary file Size Download File type/resource
GSM991821_US22502657_251507211010_S01_H_flip_4-4.avg.gpr.gz 808.0 Kb (ftp)(http) GPR
Processed data included within Sample table

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