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Sample GSM153633 Query DataSets for GSM153633
Status Public on Apr 10, 2007
Title Expression in spo11Y135F strain at meiosis 0 hr
Sample type RNA
 
Source name 0 hr after transfer into sporulation medium
Organism Saccharomyces cerevisiae
Characteristics strain: RKD1312
background: SK1
genotype: spo11Y135F
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) [email protected]
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 3.2 A 0.973889
AFFX-MurIL10_at 1.4 A 0.997725
AFFX-MurIL4_at 10.5 A 0.772364
AFFX-MurFAS_at 3.9 A 0.976071
AFFX-BioB-5_at 203.4 P 0.005565
AFFX-BioB-M_at 270.1 P 0.00006
AFFX-BioB-3_at 231.9 P 0.000127
AFFX-BioC-5_at 387.4 P 0.000857
AFFX-BioC-3_at 357.7 P 0.000147
AFFX-BioDn-5_at 515.7 P 0.000052
AFFX-BioDn-3_at 3291.2 P 0.000044
AFFX-CreX-5_at 3787.8 P 0.000044
AFFX-CreX-3_at 5430.6 P 0.000044
AFFX-BioB-5_st 17.5 A 0.5
AFFX-BioB-M_st 3.7 A 0.891021
AFFX-BioB-3_st 8.1 A 0.814869
AFFX-BioC-5_st 8.7 A 0.814869
AFFX-BioC-3_st 13.2 A 0.686277
AFFX-BioDn-5_st 14.1 A 0.5
AFFX-BioDn-3_st 58.5 P 0.026111

Total number of rows: 9335

Table truncated, full table size 226 Kbytes.




Supplementary file Size Download File type/resource
GSM153633.CEL.gz 2.0 Mb (ftp)(http) CEL

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