NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM539704 Query DataSets for GSM539704
Status Public on Nov 03, 2010
Title WT HRG 3h
Sample type RNA
 
Source name breast epithelial cell, adherent, HRG, 3h
Organism Homo sapiens
Characteristics cell line: MCF-7
tissue origination: mammary gland, breast
cell type: epithelial
disease: adenocarcinoma
age: 69
gender: female
ethnicity: Caucasian
tamoxifen phenotype: sensitive
treatment: HRG
time: 3h
Biomaterial provider American Type Culture Collection (ATCC)
Treatment protocol Following the incubation in serum-free medium, the ligand was added and incubated for the indicated time.
Growth protocol Prior to the growth factor (GF) treatment, cells were serum starved for 16-18 hours with serum-free RPMI medium and incubated at 37C/5% CO2. The medium was again changed 2 hr prior to the GF treatment.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIzol reagent (Invitrogen) and then purified using the QIAGEN Rneasy kit.
Label biotin
Label protocol Standard Affymetrix Protocols (Affymetrix GeneChip Expression Analysis Technical Manual) was used. Complete protocol can be found on the manufacturer's web site (http://www.affymetrix.com/support/technical/manual/expression_manual.affx) (section2, chapter1-p13-18, & 2.1.p32-33,p36-40).
 
Hybridization protocol Standard Affymetrix Protocols (Affymetrix GeneChip Expression Analysis Technical Manual) was used. Complete protocol can be found on the manufacturer's web site (http://www.affymetrix.com/support/technical/manual/expression_manual.affx) (section2, 2.2.p3-8 & 2.3.p3-14).
Scan protocol GeneChips were scanned using the GeneChip Scanner 3000 with default parameters.
Description Gene expression in HRG-stimulated WT cells.
wt2.HRG.03h
Data processing The data were preprocessed with RMA. Signal intensity was calculated for RefSeq mRNA by using a CustomCDF (HGU133Plus2_Hs_REFSEQ ver.11).
 
Submission date Apr 30, 2010
Last update date Nov 03, 2010
Contact name Mariko Okada
E-mail(s) [email protected]
Organization name RIKEN RCAI
Lab Laboratory for Cellular Systems Modeling
Street address W518, 1-7-22, Suehiro-cho, Tsurumi-ku
City Yokohama
ZIP/Postal code 230-0045
Country Japan
 
Platform ID GPL10371
Series (1)
GSE21618 Expression profiling of ligand-stimulated wild type and tamoxifen-resistant MCF-7

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
NR_002812_at 6.438716014
NM_182762_at 7.446275167
NM_130786_at 7.414457675
NM_014576_at 5.557479198
NM_138932_at 5.557479198
NM_138933_at 5.557479198
NM_018723_at 5.95439402
NM_145891_at 5.960789506
NM_145892_at 6.007401623
NM_145893_at 5.960789506
XM_001714498_at 5.345158094
XM_001714769_at 5.345158094
XM_001715756_at 5.345158094
NM_000014_at 5.472217729
NM_144670_at 4.284757908
NM_017436_at 7.649110057
NM_016161_at 4.964180712
NR_015356_at 5.734676303
NM_015665_at 8.937663596
NM_023928_at 9.824275987

Total number of rows: 26871

Table truncated, full table size 669 Kbytes.




Supplementary file Size Download File type/resource
GSM539704.cel.gz 8.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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