NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM556890 Query DataSets for GSM556890
Status Public on Jun 17, 2010
Title Day 7 replicate 2
Sample type RNA
 
Channel 1
Source name Day 07 908L
Organism Homo sapiens
Characteristics cell line: ZR75-1 xenograft
Treatment protocol All animals received E2. On day 0, animals were randomly allocated to tamoxifen (2.5 mg released over 60 days, Innovative Research of America) or E2 -only control groups
Growth protocol Total RNA extracted using Qiagen RNeasy kit (Qiagen, Valencia, CA, USA), according to the manufacturer’s instructions
Extracted molecule total RNA
Extraction protocol Total RNA (100ug), spiked with bacterial-RNA mixture for control was used to prepare direct Cy3- and Cy5-labelled first-strand cDNA probes using a single-base anchored oligo dT17 primer (Sigma) and Superscript II reverse transcriptase (Invitrogen). Unincorporated nucleotides were removed using QIAquick PCR purification kit (QIAGEN)
Label cy3
Label protocol Cy3- and Cy5-labelled probes were coprecipitated with 16µg human Cot 1 DNA (Invitrogen) and 8µg polyA (Sigma). The pellets were resuspended in 8 µl of H2O and 40 µl of hybridization buffer (5 X SSC, 6 X Denhardt’s solution, 60mM Tris HCl pH7.6, 0.12% sarkosyl, 48% formamide) boiled for 5 min and cooled at room temperature for 10 min.
 
Channel 2
Source name Reference Control
Organism Homo sapiens
Characteristics cell line: ZR75-1 xenograft
Treatment protocol All animals received E2. On day 0, animals were randomly allocated to tamoxifen (2.5 mg released over 60 days, Innovative Research of America) or E2 -only control groups
Growth protocol Total RNA extracted using Qiagen RNeasy kit (Qiagen, Valencia, CA, USA), according to the manufacturer’s instructions
Extracted molecule total RNA
Extraction protocol Total RNA (100ug), spiked with bacterial-RNA mixture for control was used to prepare direct Cy3- and Cy5-labelled first-strand cDNA probes using a single-base anchored oligo dT17 primer (Sigma) and Superscript II reverse transcriptase (Invitrogen). Unincorporated nucleotides were removed using QIAquick PCR purification kit (QIAGEN)
Label cy5
Label protocol Cy3- and Cy5-labelled probes were coprecipitated with 16µg human Cot 1 DNA (Invitrogen) and 8µg polyA (Sigma). The pellets were resuspended in 8 µl of H2O and 40 µl of hybridization buffer (5 X SSC, 6 X Denhardt’s solution, 60mM Tris HCl pH7.6, 0.12% sarkosyl, 48% formamide) boiled for 5 min and cooled at room temperature for 10 min.
 
 
Hybridization protocol The mix was overlaid with a coverslip and hybridised at 47°C for 12–24 h in a humidified atmosphere to Sanger Hver 1.3.1 cDNA microarrays (as part of the CRUK/LICR Microarray Consortium, contain 9930 sequence-validated cDNA clones representing approximately 6000 unique sequences). Microarrays were washed sequentially with 2x SSC, 0.1x SSC/0.1% SDS, and 0.1x SSC and were air-dried by briefly spinning in a centrifuge to remove excess liquid.
Scan protocol Fluorescent images of hybridised microarrays were captured using a ScanArray Express 3.0 scanner (Perkin Elmer) and ScanArray software
Description Technical replicate 1 of 2, Biological replicate 2 of 4. Control pool untreated.
Data processing background subtracted data obtained from log2 of processed Red signal/processed Green signal. Data was lowess normalized using the bioconductor package limma
 
Submission date Jun 16, 2010
Last update date Jun 16, 2010
Contact name Andrew H Sims
E-mail(s) andrew.sims@ed.ac.uk
Organization name University of Edinburgh
Department Institute of Genetics and Molecular Medicine
Lab Applied Bioinformatics of Cancer
Street address Systems Medicine Building
City Carrington Crescent
State/province Edinburgh
ZIP/Postal code EH4 2XR
Country United Kingdom
 
Platform ID GPL506
Series (1)
GSE22386 Dynamic changes in gene expression in vivo predict prognosis of tamoxifen-treated patients with breast cancer

Data table header descriptions
ID_REF
VALUE normalized log2 ratio test/reference

Data table
ID_REF VALUE
1028770_A -0.109390186
1028836_A -0.109897556
1030443_A 0.61161548
1030769_A 0.088390674
1030933_A 0.237504742
1030933_B 0.356715761
1033805_A 0.281428388
1035639_A -0.336955889
1046864_A 0.069115017
1048805_A 0.264128201
1049315_A 0.240470662
1049330_A 0.348737532
1055667_A 0.56961884
1055766_A 0.120946952
1056796_A -0.181089015
1058498_A -0.1175994
1058642_A -0.156761192
1058783_A -0.28495151
1059554_A -0.124301216
1059554_B -0.526231674

Total number of rows: 9928

Table truncated, full table size 206 Kbytes.




Supplementary file Size Download File type/resource
GSM556890.txt.gz 166.8 Kb (ftp)(http) TXT
Processed data included within Sample table

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