NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1024289 Query DataSets for GSM1024289
Status Public on Oct 23, 2012
Title siRNA targeted to AR exon 1 treated with ethanol, replicate 2
Sample type RNA
 
Source name late-passage CWR-R1 prostate cancer cells
Organism Homo sapiens
Characteristics cell line: CWR-R1 prostate cancer cells
genotype/variation: 48kb intragenic deletion in AR intron 1
sirna: AR exon 1
biological replicate number: rep2
agent: ethanol
Treatment protocol 48h post-transfection with the appropriate siRNA, cells were stimulated with 1nM DHT or vehicle control (ethanol) for 24h prior to RNA extraction.
Growth protocol Late-passage CWR-R1 cells were cultured in RPMI 1640 medium supplemented with penicillin/streptomycin and 5% charcoal-stripped, steroid-depleted serum for 48h following electroporation. Cells were then switched to serum-free RPMI 1640 medium supplemented with penicillin/streptomycin containing 1nM DHT or vehicle control (ethanol) for 24h.
Extracted molecule total RNA
Extraction protocol RNA was extracted using an acid guanidinium method and cleaned using a QIAGEN RNeasy kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with an a NanoDrop 8000 spectrophotometer and Caliper LabChip GX.
Label biotin
Label protocol Total RNA was converted to amplified, biotinylated, antisense cRNA using the Illumina TotalPrep-96 RNA Amplification Kit (Life Technologies) in accordance with the manufacturer's specifications.
 
Hybridization protocol 150ng of biotin-labeled cRNA was hybridized with Illumina Beadchips using the HumanHT-12 v4 Expression Beadchip Kit in accordance with the manufacturer's specifications.
Scan protocol Hybridized Beadchips were scanned with an Illumina iScan.
Description SAMPLE 11
Data processing Average probe intensity data was extracted from iScan image files using the Partek Report Plug-in for Illumina GenomeStudio and then imported to Partek Genomics Suite 6.6. Raw intensity data was log2 transformed and quantile normalized using Partek GS 6.6.
 
Submission date Oct 23, 2012
Last update date Oct 23, 2012
Contact name Scott Dehm
E-mail(s) dehm@umn.edu
Organization name Masonic Cancer Center, University of Minnesota
Street address Mayo Mail Code 806, 420 Delaware St SE
City Minneapolis
ZIP/Postal code 55455
Country USA
 
Platform ID GPL10904
Series (1)
GSE41784 Androgen receptor splice variants mediate enzalutamide resistance in castration-resistant prostate cancer cell lines

Data table header descriptions
ID_REF
VALUE log2 transformed, quantile normalized average probe intensity
Detection Pval

Data table
ID_REF VALUE Detection Pval
7A5 6.50992
A1BG 6.71065
A1CF 6.59474
A26C3 6.60194
A2BP1 6.52482
A2LD1 8.07469
A2M 6.51481
A2ML1 6.39067
A3GALT2 6.47247
A4GALT 6.73479
A4GNT 6.74484
AAA1 6.52948
AAAS 7.41269
AACS 8.13339
AACSL 6.69675
AADAC 6.58055
AADACL1 7.31757
AADACL2 6.55877
AADACL3 6.44446
AADACL4 6.73012

Total number of rows: 34693

Table truncated, full table size 577 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap