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Sample GSM143913 Query DataSets for GSM143913
Status Public on Nov 10, 2006
Title ME-A cells: breast cancer cell line
Sample type RNA
 
Source name breast cancer cell line
Organism Mus musculus
Characteristics Small tissue segments from the 583 tumor 1 were isolated and used to establish the ME-A cells. These cells show continuous T/t-antigen synthesis and are permanently T/t-antigen positive. They exhibit the morphology and growth characteristics of tumor cells.
Extracted molecule total RNA
Extraction protocol RNA was isolated from mammary gland tissue segments stored in liquid nitrogen. The frozen tissue segments were ground to a fine powder using a liquid nitrogen chilled mortar and pestle. Total RNA was extracted with RNAzol reagent in accordance with the manufacturer’s protocol (PeQLab, Biotechnology), and the isolated RNA was treated with RNasefree DNase (DNA-free Ambion, Austin, Tex., USA). The integrity of RNA was verified with the Agilent Bioanalyzer (Agilent Technologies) by the presence of prominent 28S and 18S bands on agarose gels and an A260/280 ratio in the range of 1.9–2.1.
Label biotin
Label protocol The dsDNA was in vitro transcribed into biotinylated cRNA by RNA Transcript labeling Kit (Enzo Life Sciences, Inc).
 
Hybridization protocol The Affymetrix GeneChip was hybridized with the biotin-labelled cRNA fragments for 16 hr at 45°C. Washing steps for the chip, staining with streptavidin-phycoerythrin and signal-amplification were performed according to the manufacturer’s instructions.
Scan protocol Each hybridized Affymetrix GeneChip array was scanned with GeneChip Scanner 3000.
Description see: Klein A, Guhl E, Zollinger R, Tzeng YJ, Wessel R, Hummel M, Graessmann M, Graessmann A. Gene expression profiling: cell cycle deregulation and aneuploidy do not cause breast cancer formation in WAP-SVT/t transgenic animals. J Mol Med. 2005 May;83(5):362-76.
Data processing The raw experimental microarray data were normalized with the Affymetrix Microarray Suite (MAS 5.0) based on the housekeeping gene method. Further analyses were performed with the software CorrXpression.
 
Submission date Nov 08, 2006
Last update date Nov 09, 2006
Contact name Andreas Klein
E-mail(s) [email protected]
Phone +49 30 450 528087
Fax +49 30 450 52945
URL http://www.charite.de/molbiol/bioinf/tumbiol/
Organization name Charité (CCO)
Department Institute of Biochemistry
Street address Charitéplatz 1
City Berlin
ZIP/Postal code 10117
Country Germany
 
Platform ID GPL339
Series (1)
GSE6246 Gene expression profiling: breast cancer formation in WAP-SVT/t transgenic animals

Data table header descriptions
ID_REF
VALUE ME-A cells
ABS_CALL ME-A cells
DETECTION P-VALUE ME-A cells

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 125 P 0.011384
AFFX-BioB-M_at 173.2 P 0.000169
AFFX-BioB-3_at 83.5 P 0.002556
AFFX-BioC-5_at 271.7 P 0.000446
AFFX-BioC-3_at 193.1 P 0.000081
AFFX-BioDn-5_at 243.8 P 0.000127
AFFX-BioDn-3_at 1652.7 P 0.000581
AFFX-CreX-5_at 2876.5 P 0.000044
AFFX-CreX-3_at 4395 P 0.000044
AFFX-DapX-5_at 13.5 A 0.205732
AFFX-DapX-M_at 22.3 A 0.165861
AFFX-DapX-3_at 4.6 A 0.824672
AFFX-LysX-5_at 3.3 A 0.804734
AFFX-LysX-M_at 3.1 A 0.737173
AFFX-LysX-3_at 10 A 0.089478
AFFX-PheX-5_at 2.6 A 0.843268
AFFX-PheX-M_at 11.3 A 0.645547
AFFX-PheX-3_at 24.2 A 0.425962
AFFX-ThrX-5_at 2.8 A 0.834139
AFFX-ThrX-M_at 17 A 0.313723

Total number of rows: 22690

Table truncated, full table size 616 Kbytes.




Supplementary file Size Download File type/resource
GSM143913.CEL.gz 3.6 Mb (ftp)(http) CEL

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