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Sample GSM153634 Query DataSets for GSM153634
Status Public on Apr 10, 2007
Title Expression in spo11Y135F strain at meiosis 4 hr
Sample type RNA
 
Source name 4 hrs 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). The cells were suspended in sporulation medium (1% potasium acetate, 1/5 level of amino acids, and polypropylene glycol) to a density of 2x10^7 cells/ml, and incubated for 4 hrs at 30C for sporulation.
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 prophase.
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings. The comparison with GSM153627 was performed with MAS 5.0 using Affymetrix default analysis settings. See Comparison data table on Series GSE6620 record.
 
Submission date Dec 29, 2006
Last update date Jan 03, 2007
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 3.3 A 0.987453
AFFX-MurIL10_at 1.1 A 0.996788
AFFX-MurIL4_at 2.5 A 0.978098
AFFX-MurFAS_at 13.8 A 0.60308
AFFX-BioB-5_at 176.1 P 0.002023
AFFX-BioB-M_at 292.3 P 0.000052
AFFX-BioB-3_at 199.2 P 0.00011
AFFX-BioC-5_at 464.2 P 0.000081
AFFX-BioC-3_at 309.7 P 0.000095
AFFX-BioDn-5_at 484.5 P 0.000044
AFFX-BioDn-3_at 3097.1 P 0.000044
AFFX-CreX-5_at 3615.6 P 0.000044
AFFX-CreX-3_at 5648.4 P 0.000044
AFFX-BioB-5_st 32.1 A 0.340661
AFFX-BioB-M_st 6.1 A 0.824672
AFFX-BioB-3_st 6.2 A 0.883887
AFFX-BioC-5_st 15.1 A 0.804734
AFFX-BioC-3_st 27.6 A 0.470241
AFFX-BioDn-5_st 15.1 A 0.617401
AFFX-BioDn-3_st 76 P 0.033677

Total number of rows: 9335

Table truncated, full table size 226 Kbytes.




Supplementary file Size Download File type/resource
GSM153634.CEL.gz 2.0 Mb (ftp)(http) CEL

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