NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM297717 Query DataSets for GSM297717
Status Public on Jun 12, 2008
Title Tamoxifen treated vector control, biological rep 1
Sample type RNA
 
Source name NIH3T3 retrovirally transduced with pBabe-puro control vector
Organism Mus musculus
Characteristics NIH3T3 (p16/p19arf null) confluent cell cultures, harvested after 24hrs treatment
Treatment protocol All samples were treated with ethanol alone (0.2%) or 4-OHT tamoxifen (0.1mM) in ethanol for 24 hours prior to RNA extraction.
Growth protocol All cultures were grown to confluence (7 days) in DMEM under standard conditions. The raw data were generated with GeneChip Operating Software (GCOS). Data was normalised with Robust Multichip Average (RMA) method using Bioconductor module Affy implemented into the automated FunAlyse pipeline in the Sir Henry Wellcome Functional Genomics Facility
Extracted molecule total RNA
Extraction protocol RNA was extracted using Rneasy Mini kit (Qiagen) according to the manufacturers' protocol
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Genome 430 2.0 Array in the GeneChip Hybridization Oven 640. Arrays were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol Arrays were scanned using the GeneChip Scanner 3000 7G.
Description Comparative study of gene targets regulated by overexpression of the different Runx family members
Data processing The raw data were generated with GeneChip Operating Software (GCOS). Data was normalised with Robust Multichip Average (RMA) method using Bioconductor module Affy implemented into the automated FunAlyse pipeline in the Sir Henry Wellcome Functional Genomics Facility. Differential expression was calculated using RankProducts method.
 
Submission date Jun 10, 2008
Last update date Aug 28, 2018
Contact name Pawel Herzyk
E-mail(s) pawel.herzyk@glasgow.ac.uk
Phone 00441413303180
Organization name University of Glasgow
Department College of Medical, Veterinary and Life Sciences
Lab Glasgow Polyomics
Street address Wolfson Wohl Cancer Research Centre, Garscube Estate
City Bearsden
ZIP/Postal code G61 1QH
Country United Kingdom
 
Platform ID GPL1261
Series (1)
GSE11732 Runx transcriptional program for control of cell adhesion and survival
Relations
Reanalyzed by GSE119085

Data table header descriptions
ID_REF
VALUE RMA generated log2 expression values

Data table
ID_REF VALUE
1415670_at 8.628386605
1415671_at 8.897179813
1415672_at 8.737644071
1415673_at 7.907291099
1415674_a_at 7.504249657
1415675_at 7.314731652
1415676_a_at 9.491569011
1415677_at 7.566791517
1415678_at 8.874324742
1415679_at 9.577652784
1415680_at 8.384932416
1415681_at 8.516809021
1415682_at 6.726774919
1415683_at 9.157495519
1415684_at 6.954858761
1415685_at 7.241492092
1415686_at 7.958489229
1415687_a_at 11.22335631
1415688_at 8.477496418
1415689_s_at 5.41923062

Total number of rows: 45101

Table truncated, full table size 1026 Kbytes.




Supplementary file Size Download File type/resource
GSM297717.CEL.gz 3.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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