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Sample GSM60552 Query DataSets for GSM60552
Status Public on Nov 14, 2005
Title C-Line-C7R1dim-high-6h-GC
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 dexamethansone 10e-7M 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 dexamethansone 10e-7M 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) [email protected]
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 20.3003120623569
1053_at 242.654532841855
117_at 16.2325753374561
121_at 109.548050472995
1255_g_at 4.69700132313567
1294_at 69.9348667326374
1316_at 16.5004103694342
1320_at 11.3119833761896
1405_i_at 4.60873239389293
1431_at 9.17361270201994
1438_at 13.1303184384616
1487_at 76.6296069122696
1494_f_at 17.6106957245734
1552256_a_at 127.107909764569
1552257_a_at 323.407651117838
1552258_at 9.04907294970323
1552261_at 12.7892521486506
1552263_at 58.009609398052
1552264_a_at 313.319336903395
1552266_at 5.25816713541044

Total number of rows: 54675

Table truncated, full table size 1480 Kbytes.




Supplementary file Size Download File type/resource
GSM60552.CEL.gz 7.4 Mb (ftp)(http) CEL

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