NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM470537 Query DataSets for GSM470537
Status Public on Feb 23, 2010
Title Sp-H2O2-Biorep2
Sample type RNA
 
Source name Wildtype S.pombe strain
Organism Schizosaccharomyces pombe 972h-
Characteristics oxidative stress: yes
Treatment protocol Two separate cultures developed from independent single colonies were processed in parallel throughout the entire experiment (biological duplicates). Cells from a 30 ml volume were collected by centrifugation at 2000 rpm for 2 minutes and the pellet was frozen immediately in liquid nitrogen (control samples). Hydrogen peroxyde (SIGMA, H-1009) was added to the rest of the culture at a final concentration of 0.5 mM and incubation proceed for 30 minutes after which 30 ml of culture were processed as above
Growth protocol 100 ml yeast extract (YE) medium at 30 ºC and 170 rpm until OD595=0.2 (4 X 106 cells/ml)
Extracted molecule total RNA
Extraction protocol Total RNA was prepared by resuspending the cell pellets in 20 μl extraction buffer (100 mM EDTA pH 8.0, 100 mM NaCl, 50 mM Tris-Hcl pH 8.0), 20 μl phenol/chloroform, 2 μl 10% SDS, 200 μl glass beads (425-600 μm, SIGMA G-8772). Cells were mechanically disrupted in a Fast-Prep (Savant BIO 101) and the cell lysate was extracted with phenol, phenol/chloroform and chloroform/isoamyl alcohol before precipitation with 0.3 M sodium acetate and ethanol. RNA was resuspended in 50 μl of sterile water with Diethyl pyrocarbonate (SIGMA D-5758) and was furher purified through a RNeasy mini kit (Quiagen) following the suppliers specifications.
Label biotin
Label protocol Target labeling preserving the original polarity of RNAs was performed following the instructions of the GeneChip whole transcript sense target labelling assay manual from Affymetrix.
 
Hybridization protocol Platform hybridization was performed using 5 micrograms of single stranded sense DNA, labelled with biotin and fragmented to an average size of 100 nucleotides. Hybridization was performed following the instructions of the Affymetrix assay manual for each platform.
Scan protocol Affymetrix standard protocol using Affymetirix Fluidics 450 and Scanner 3000
Description Platform GPL7715-CustomCDF
Data processing RMA
 
Submission date Nov 13, 2009
Last update date Feb 22, 2010
Contact name Luis Quintales
Organization name Instituto de Biología Funcional y Genómica (IBFG)
Department Universidad de Salamanca / CSIC
Street address Calle Zacarías González, 2
City Salamanca
ZIP/Postal code 37007
Country Spain
 
Platform ID GPL9672
Series (1)
GSE19020 Analysis of DNA strand-specific differential expression with high density tiling microarrays

Data table header descriptions
ID_REF
VALUE log2 RMA signal intensity

Data table
ID_REF VALUE
aah2:SPAC23D3.14c 7.3453
aah3:SPCC63.02c 11.5616
aap1:SPBC16A3.20c:SPBC1652.02 11.765
aar2:SPAC3H5.04 9.7763
abc1:coq8:SPBC2D10.18 9.8087
abc3:SPBC359.05 10.7395
abc4:SPAC30.04c 11.9375
abp2:SPBC1861.02 10.8639
ace2:SPAC6G10.12c 8.8961
acp1:SPAC12B10.07 9.3852
acp2:SPAC631.01c 12.6241
ada1:SPBC106.04 11.1436
ada2:SPCC24B10.08c 10.1143
ade1:min4:SPBC4C3.02c:SPBC405.01 12.2723
ade10:SPCPB16A4.03c 13.3988
ade2:min10:min3:SPAC144.03 11.6288
ade3:min11:SPAC6F12.10c 13.0091
ade4:min13:aza1:SPAC4D7.08c 13.2566
ade5:ade8:SPCC569.08c 11.3992
ade6:min1:SPCC1322.13 12.0564

Total number of rows: 4856

Table truncated, full table size 117 Kbytes.




Supplementary file Size Download File type/resource
GSM470537_Sp-TMA-OX-2.CEL.gz 10.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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