NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM253520 Query DataSets for GSM253520
Status Public on May 29, 2009
Title Δrsf1 YPG30min biological-rep1
Sample type RNA
 
Source name isogenic Δrsf1 mutant yeast grown to A600=0.6 in YPD then switched to YPG for 30 minutes
Organism Saccharomyces cerevisiae
Characteristics strain: isogenic Δrsf1 mutant
Treatment protocol Cells grown to A600 = 0.6 in 50 ml of rich medium containing dextrose as sole carbon source were collected by centrifugation, washed 2x in YPG and resupended in YPG prewarmed to 30ºC and incubated for the specified number of minutes
Growth protocol Cells grown to A600 = 0.6 in 50 ml of rich medium containing dextrose, glycerol or ethanol as sole carbon source
Extracted molecule polyA RNA
Extraction protocol total nucleic acids were extracted using the "hot phenol extraction" method (McEntee and Hudson, Anal Biochem. 1989 176(2):303-6.) PolyA mRNA was prepared according to oligotex manual specifications.
Label biotin
Label protocol 1 µg ds cDNA was labeled according to Affymetrix manual specifications.
 
Hybridization protocol Following fragmentation, 15 µg of cRNA were hybridized for 16 hours at 37ºC. Fragmentation and hybridization were performed at the MSU Research Tecnhology Support
Scan protocol Gene Chips were scanned in a high density GC3000 scanner using GCOS operating software
Description Rsf1p is required for an efficient metabolic shift from fermentative to glycerol-based respiratory growth in S cerevisiae (submitted)
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0). Median of each chip scaled to 500, values less than 0.01 set to 0.01. MSU Research Tecnhology
 
Submission date Dec 27, 2007
Last update date May 25, 2011
Contact name George Gordon Roberts III
Organization name Wayne State University
Department Immunology/Microbiology
Lab Hudson
Street address 540 E. Canfield
City Detroit
State/province MI
ZIP/Postal code 48201
Country USA
 
Platform ID GPL90
Series (1)
GSE10031 mRNA expression data in Δrsf1mutant during growth on, and transition to growth on glycerol as sole carbon source

Data table header descriptions
ID_REF
VALUE MAS 5.0 signal
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
10000_at 9.8 P 0.031336
10001_at 219.3 P 0.000266
10002_i_at 1089.3 A 0.25
10003_f_at 4123.1 P 0.000219
10004_at 0.6 A 0.97214
10005_at 406.3 P 0.000219
10006_at 86.1 P 0.001892
10007_at 263.3 P 0.000322
10008_at 27.2 A 0.204022
10009_at 14.6 A 0.302547
10010_at 1784.7 P 0.000219
10011_at 4.3 A 0.5
10012_at 33.1 P 0.002617
10013_at 214 P 0.000219
10014_at 266.2 P 0.000219
10015_at 295.2 P 0.000468
10016_at 1539.5 P 0.000219
10017_at 2 A 0.92617
10018_at 9.1 A 0.438361
10019_at 822 P 0.000219

Total number of rows: 9335

Table truncated, full table size 226 Kbytes.




Supplementary file Size Download File type/resource
GSM253520.CEL.gz 1.9 Mb (ftp)(http) CEL
GSM253520.chp.gz 2.9 Mb (ftp)(http) CHP
Processed data provided as supplementary file
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap