NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM297713 Query DataSets for GSM297713
Status Public on Jun 12, 2008
Title Tamoxifen treated (induced) RUNX1-ER, biological rep 1
Sample type RNA
 
Source name NIH3T3 retrovirally transduced with inducible Human RUNX1 construct in pBabe-puro
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 8.609236143
1415671_at 9.069110978
1415672_at 8.680041808
1415673_at 7.585478239
1415674_a_at 7.408148909
1415675_at 7.149893419
1415676_a_at 9.529398788
1415677_at 7.185106726
1415678_at 8.920793015
1415679_at 9.620200079
1415680_at 8.4126869
1415681_at 8.627031358
1415682_at 6.96007042
1415683_at 9.051296689
1415684_at 7.138218607
1415685_at 7.042824155
1415686_at 8.073831875
1415687_a_at 11.40845242
1415688_at 8.452172559
1415689_s_at 5.575192528

Total number of rows: 45101

Table truncated, full table size 1026 Kbytes.




Supplementary file Size Download File type/resource
GSM297713.CEL.gz 3.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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