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Sample GSM153631 Query DataSets for GSM153631
Status Public on Apr 10, 2007
Title Expression in rad50delta strain at meiosis 0 hr
Sample type RNA
 
Source name 0 hr after transfer into sporulation medium
Organism Saccharomyces cerevisiae
Characteristics strain: RKD101
background: SK1
genotype: rad50delta
Treatment protocol Cells were washed twice with water, frozen in liquid nitrogen, and stored at -80C.
Growth protocol Cells were grown on a YPD plate for 2 days at 30C. The cells were grown to a density of 4.0x10^7 cells/ml at 30C in SPS presporulation medium (0.5% yeast extract, 1% peptone, 0.17% yeast nitrogen base w/o amino acid and ammonium sulfate, 1% potassium acetate, 0.5% ammonium sulfate, usual level fo amino acids, 50 mM potassium phthalate buffer pH 5.0, and antifoam).
Extracted molecule polyA RNA
Extraction protocol Total RNA was prepared using glass beads and RNeasy Maxi Kit (QIAGEN). mRNA was isolated the total RNA using Oligotex-dT30 (TaKaRa). These processes were performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 3 microg mRNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 microg of cRNA were hybridized for 16 hr at 45C on GeneChip YG-S98. GeneChips were washed and stained using EukGE-WS1 ver3 protocol in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
Description Gene expression data from diploid cells in premeiosis.
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings.
 
Submission date Dec 29, 2006
Last update date Dec 29, 2006
Contact name Kazuto Kugou
E-mail(s) kkugou@kazusa.or.jp
Organization name Kazusa DNA Research Institute
Department Department of Frontier Research
Lab Laboratory of Cell Engineering
Street address 2-6-7 KazusaKamatatri
City Kisarazu
State/province Chiba
ZIP/Postal code 292-0818
Country Japan
 
Platform ID GPL90
Series (1)
GSE6620 Expression data from wild type, mre11delta, rad50delta, and spo11Y135F at meiosis 0 hr and 4 hr.

Data table header descriptions
ID_REF
VALUE MAS5-calculated Signal intensity
ABS_CALL the call in an absolute analysis that indicates if the transcript was present (P), absent (A), marginal (M), or no call (NC)
DETECTION P-VALUE detection p-value', p-value that indicates the significance level of the detection call

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-MurIL2_at 6.6 A 0.834139
AFFX-MurIL10_at 3 A 0.976071
AFFX-MurIL4_at 1 A 0.910522
AFFX-MurFAS_at 2.7 A 0.957038
AFFX-BioB-5_at 139.8 P 0.000857
AFFX-BioB-M_at 309.2 P 0.000169
AFFX-BioB-3_at 269.5 P 0.000081
AFFX-BioC-5_at 384.8 P 0.00034
AFFX-BioC-3_at 382 P 0.000044
AFFX-BioDn-5_at 481.7 P 0.000044
AFFX-BioDn-3_at 3181.7 P 0.000044
AFFX-CreX-5_at 4359.9 P 0.000044
AFFX-CreX-3_at 6418.8 P 0.000044
AFFX-BioB-5_st 4.1 A 0.749204
AFFX-BioB-M_st 6.4 A 0.868639
AFFX-BioB-3_st 7.8 A 0.834139
AFFX-BioC-5_st 8 A 0.852061
AFFX-BioC-3_st 18.4 A 0.440646
AFFX-BioDn-5_st 28.2 A 0.51489
AFFX-BioDn-3_st 45.5 A 0.095667

Total number of rows: 9335

Table truncated, full table size 225 Kbytes.




Supplementary file Size Download File type/resource
GSM153631.CEL.gz 2.0 Mb (ftp)(http) CEL

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