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Sample GSM742086 Query DataSets for GSM742086
Status Public on Jun 30, 2011
Title Control 0 hour no tetracycline rep2
Sample type RNA
 
Source name mammary
Organism Mus musculus
Characteristics cell line: 3134
receptor: MGI 7035
source strain: RIII
gender: female
time: 0 hour
treatment: control
tet-off: no tetracycline
transgene: A-fos (AP1 dominant negative) and the tetracycline regulator (tTa)
Biomaterial provider Hager;hager-lab
Treatment protocol Control, untreated 0 hour with tetracycline (1ug/ml)
Growth protocol Cell lines were maintained in Dulbecco's Modified Eagle Medium (DMEM) (Invitrogen, Carlsbad, CA) supplemented with 10% fetal bovine serum (Gemini, Woodland, California), 2 mM L-glutamine, 1 mM sodium pyruvate, 0.1 mM non-essential amino acids, 5 mg/ml penicillin-streptomycin (Invitrogen, Carlsbad, CA) and kept at 37ºC incubator with 5% CO2. Cells were transferred to 10% charcoal-dextran-treated, heat-inactivated fetal bovine serum for 48 hrs prior to hormone treatment.
Extracted molecule total RNA
Extraction protocol RNA was extracted from cells either vehicle treated or treated with 100 nM hormone (dexamethasone, Dex) for 0h, 2h, 4h or 8h. 3134 and AtT-20 RNA for microarray analysis was prepared via standard manufacturer protocols (Qiagen, Valencia, Ca) using cells resuspended in Trizol reagent (Invitrogen, Carlsbad, Ca)
Label biotin
Label protocol RNA from untreated and dex treated cells were labeled with biotin-CTP using manufacturer's recommendations (Affymetrix, Santa Clara, Ca)
 
Hybridization protocol Hybridizations were carried out according the manufacturer (Affymetrix) protocol.
Scan protocol Affymterix Gene Chip Scanner 3000
Description mouse mammary adenocacinoma tumor with A-fos stably integrated male. The 3134 cell line was derived by transformation of C127, originally isolated from a mammary adenocacinoma tumor of the RIII mouse. A-fos (AP1 dominant negative) and the tetracycline regulator (tTa) were stably integrated into the 3134 cell line., dexamethasone 0 hour control
Dexamethasone untreated, 0 hour control.
Data processing Probe-level CEL files were processed through Affymetrix Expression Console using RMA summarization and median normalization methods.
MoGene-1_0-st-v1.r4.pgf
 
Submission date Jun 15, 2011
Last update date Jun 30, 2011
Contact name John A Stamatoyannopoulos
E-mail(s) [email protected]
Organization name Altius Institute / University of Washington
Department Genome Sciences
Lab Stamatoyannopoulos
Street address 2211 Elliott Avenue, 6th Floor
City SEATTLE
State/province WA
ZIP/Postal code 98121
Country USA
 
Platform ID GPL6246
Series (1)
GSE29983 Comparison of gene expression profiles for hormone induction in the presence and absence of AP1 binding.

Data table header descriptions
ID_REF
VALUE RMA summarization and median normalization log intensities

Data table
ID_REF VALUE
10564011 2.393708
10563935 2.191174
10563937 2.399101
10564041 2.326761
10564089 2.445053
10564111 2.041091
10564147 2.191571
10564073 2.236695
10564135 2.236695
10564139 2.508526
10564013 2.257513
10563923 2.785686
10564033 2.448968
10563949 2.156744
10563955 2.543783
10564137 2.55951
10564023 2.666777
10564043 2.109057
10564019 2.083881
10563943 2.156114

Total number of rows: 28888

Table truncated, full table size 504 Kbytes.




Supplementary file Size Download File type/resource
GSM742086_021909hager9MG10ST_MoGene-1_0-st-v1_+T-D.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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