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Sample GSM60551 Query DataSets for GSM60551
Status Public on Nov 14, 2005
Title C-Line-C7R1dim-high-6h-EtOH
Sample type RNA
 
Source name C7R1 dim-high cell line
Organism Homo sapiens
Characteristics homo sapiens, CCRF-CEM (ATCC no.: CLL-119) subclone C7R1 (=GC-resistant) transfected with a dimerization deficient Glucocorticoid-receptor-mutant, high expression of mutant resulting in a restored GC-sensitivity, cultured under standard conditions (37°C, 5% CO2, saturated humidity), in the presence of ethanol 0,1% for 6h
Growth protocol cultured under standard conditions (37°C, 5% CO2, saturated humidity)
Extracted molecule total RNA
Extraction protocol For total RNA isolation, TRIreagent (MRC Inc., Cincinnati, OH,USA) was used according to the manufacturer’s protocol. Briefly, up to 1x10E7 cells per ml were lysed with TRIreagent, 200ul of chloroform were added, the mixture centrifuged, and the RNA from the aqueous phase precipitated with isopropanol. The pelleted RNA was washed in 70% ethanol in DEPC-water and resuspended in nuclease-free water. RNA quantity and purity was determined by optical densitiy measurements (OD260/280) and RNA inte Glucocorticoid-receptority by using the 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA,USA), and only high quality RNA was further processed.
Label R-Phycoerythrin
Label protocol The chips were stained and washed in an Affymetrix fluidic station 450 following the EukGE-ws2v4 protocol.
 
Hybridization protocol On rotation (60 rpm) hybridization at 45C for 16 hours
Scan protocol Fluorescence signals were recorded by an Affymetrix scanner 3000 and image analysis performed with the GCOS software (version 1.2).
Description biological source: homo sapiens, CCRF-CEM (ATCC no.: CLL-119) subclone C7R1 (=GC-resistant) transfected with a dimerization deficient Glucocorticoid-receptor-mutant, high expression of mutant resulting in a restored GC-sensitivity, cultured under standard conditions (37°C, 5% CO2, saturated humidity), in the presence of ethanol 0,1% for 6h
Data processing Data processing and analysis was performed in R using Bioconductor version 1.5. GeneChip raw expression values were normalized and summarized using the robust multiarray analysis (RMA) method proposed by R. Irizarry.
 
Submission date Jun 09, 2005
Last update date Aug 28, 2018
Contact name Johannes Rainer
E-mail(s) johannes.rainer@eurac.edu
Organization name Eurac Researc
Department Institute for Biomedicine
Lab Biomedical Informatics
Street address Via A. Volta 21
City Bolzano
ZIP/Postal code 39100
Country Italy
 
Platform ID GPL570
Series (1)
GSE2842 Additional systems to Prednisolone treated childhood ALL samples
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE RMA normalized expression values

Data table
ID_REF VALUE
1007_s_at 22.2054207077245
1053_at 272.592111009055
117_at 17.1203465505888
121_at 96.1603338698564
1255_g_at 4.38318630150504
1294_at 72.1256244859928
1316_at 18.5506778575406
1320_at 9.74201361887965
1405_i_at 4.95800594046666
1431_at 12.8374788983691
1438_at 14.6232289263419
1487_at 97.7686481746843
1494_f_at 16.7303996120167
1552256_a_at 234.393702679583
1552257_a_at 540.938210809108
1552258_at 11.0693607154613
1552261_at 13.1837601861501
1552263_at 57.525511443558
1552264_a_at 256.161526504374
1552266_at 4.38112081692192

Total number of rows: 54675

Table truncated, full table size 1479 Kbytes.




Supplementary file Size Download File type/resource
GSM60551.CEL.gz 7.5 Mb (ftp)(http) CEL

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