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Sample GSM153627 Query DataSets for GSM153627
Status Public on Apr 10, 2007
Title Expression in wild type strain at meiosis 0 hr
Sample type RNA
 
Source name 0 hr after transfer into sporulation medium
Organism Saccharomyces cerevisiae
Characteristics strain: MJL1720
background: SK1
genotype: wt
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 Trizol reagent (Invitrogen). 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 6.7 A 0.834139
AFFX-MurIL10_at 1.1 A 0.963431
AFFX-MurIL4_at 1 A 0.994435
AFFX-MurFAS_at 12.4 A 0.772364
AFFX-BioB-5_at 201 P 0.000662
AFFX-BioB-M_at 261.6 P 0.000044
AFFX-BioB-3_at 240.5 P 0.000581
AFFX-BioC-5_at 360.1 P 0.000581
AFFX-BioC-3_at 292.8 P 0.000095
AFFX-BioDn-5_at 422.7 P 0.000052
AFFX-BioDn-3_at 3479 P 0.000044
AFFX-CreX-5_at 3307 P 0.000044
AFFX-CreX-3_at 5334.7 P 0.000044
AFFX-BioB-5_st 15.7 A 0.724854
AFFX-BioB-M_st 8 A 0.824672
AFFX-BioB-3_st 3.6 A 0.9273
AFFX-BioC-5_st 8.4 A 0.772364
AFFX-BioC-3_st 2.9 A 0.760937
AFFX-BioDn-5_st 74.2 A 0.300606
AFFX-BioDn-3_st 59.3 A 0.083592

Total number of rows: 9335

Table truncated, full table size 225 Kbytes.




Supplementary file Size Download File type/resource
GSM153627.CEL.gz 2.0 Mb (ftp)(http) CEL

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