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Sample GSM1109815 Query DataSets for GSM1109815
Status Public on Nov 25, 2013
Title PC-3_Icilin, rep3
Sample type RNA
 
Source name Prostate cancer cell line PC-3, icilin
Organism Homo sapiens
Characteristics cell line: PC-3
cell type: androgen-independent prostate carcinoma cell line
treatment: icilin
Treatment protocol Compounds were dissolved in ethanol as a vehicle at 0.1% working concentration and treated in PC-3 cells. Vehicle-treated PC-3 cells were used as a control.
Growth protocol The cells were maintained under DMEM medium containing 10% FBS.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from the cells and processed according to the manufacturer's guideline (Affymetrix).
Label biotin
Label protocol The Affymetrix GeneChip® procedure for generation of the biotin-labeled single-stranded cDNA by in vitro transcription were performed according to the manufacturer's instructions from 300ng total RNA (GeneChip® Whole Transcript (WT) Sense Target Labeling Assay Rev.5). Protocol was performed using the Whole Transcript Sense Target Labeling and Control Reagents (Affymetrix 900652).
 
Hybridization protocol Following fragmentation, 5.5 ug of framented cDNA were hybridized for about 17 hr at 45℃ on Human Gene 1.0 ST arrays. The hybridized probe arrays were stained and washed with the GeneChip® Hybridization, Wash and Stain Kit using the Fluidics Station 450 (Affymetrix).
Scan protocol The stained GeneChips were scanned with a GeneChip® Scanner 3000+ 7G (Affymetrix) at 570 nm.
Description icilin effect on gene expression profile in PC-3 cells.
Data processing Raw data were normalized using the Single Channel Array Normalization (Piccolo et al. 2012, PMID: 22959562) method, which is implemented as a Bioconductor package (http://www.bioconductor.org/packages/release/bioc/html/SCAN.UPC.html). As part of the normalization process, a custom chip-definition (CDF) file from the BrainArray resource was used to map genes based on updated genome mappings and excludes inaccurate or wrongly annotated probes. Microarray probes to 11,931 genes.
 
Submission date Mar 27, 2013
Last update date Mar 12, 2020
Contact name Ju-Hong Jeon
E-mail(s) [email protected]
Organization name Seoul National University College of Medicine
Department Department of Physiology and Biomedical Sciences
Lab Smooth muscle lab
Street address 28 Yongon-Dong, Chongno-Gu
City Seoul
State/province Seoul
ZIP/Postal code 110-799
Country South Korea
 
Platform ID GPL15034
Series (1)
GSE45567 The transcriptional network for cell cycle regulation in prostate cancer

Data table header descriptions
ID_REF
VALUE Normalized log2 signal intensity

Data table
ID_REF VALUE
100009676_at 0.822466506
10000_at 1.68291833
10001_at 1.880039516
10002_at -0.079753435
100033413_at 0.201883415
100033414_at 0.239758854
100033416_at 0.244033667
100033418_at 0.071496497
100033420_at 0.075291399
100033422_at 0.003581536
100033423_at -0.078181361
100033424_at 0.012971469
100033425_at -0.00185608
100033426_at 1.102487356
100033427_at 1.640374025
100033428_at -0.106592739
100033430_at 0.008955448
100033431_at 0.436990707
100033432_at 1.188921094
100033433_at 0.141444272

Total number of rows: 19738

Table truncated, full table size 407 Kbytes.




Supplementary file Size Download File type/resource
GSM1109815_PC-3_Icilin3.CEL.gz 4.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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