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Sample GSM567169 Query DataSets for GSM567169
Status Public on Mar 07, 2012
Title Total RNA upon miR-203 reconstitution in LNCaP, biological replicate 2
Sample type RNA
 
Source name Total RNA in prostate cancer cell line LNCaP upon miR-203 reconstitution
Organism Homo sapiens
Characteristics cell line: LNCaP
tissue: prostate cancer
tumor stage: early
Treatment protocol Cells were transfected using the Nucleofector 2 Technology (Amaxa) according to the instructions. For miRNA reconstitution 2.5ug plasmid DNA for each miRNA was used. AGO2 RNA co-immunoprecipitation (AGO2 co-IP) was performed using AG02-1 11A antibody (Ascenion).
Growth protocol Cells were grown in medium to confluency (LNCaP cells: RPMI 1640 medium with L-glutamine (PAA) (10%FCS (Biochrom), 100Units/ml penicillin, 100 µg/ml streptomycin (PAA) and 10mM HEPES buffer (Biochrom), PC-3 and Du-145 cells: DMEM/F-12 medium with L-glutamine (PAA) (10\%FCS (Biochrom), 100Units/ml penicillin, 100 µg/ml streptomycin (PAA)), and RWPE-1 cells: Keratinocyte-Serum free medium (Gibco-BRL) (5ng/ml human recombinant EGF and 0.05mg/ml bovine pituary extract (Gibco-BRL))).
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol 2µg RNA were analyzed on Affymetrix GeneChip Human Genome U133A 2.0 Arrays according to the manufacturer`s protocol.
 
Hybridization protocol GeneChips were proceed using the Affymetrix GCS3000 7G system according to manufacturer`s protocol.
Scan protocol GeneChips were proceed using the Affymetrix GCS3000 7G system according to manufacturer`s protocol.
Description For identifying direct targets of miR-203 a AGO2-RNA co-immunoprecipitation as described by (Beitzinger et al. 2007) was performed. Total mRNAs were identified by using Affymetrix Genechips.
Data processing The data were analyzed with R (version 2.9.0) and BioConductor (version 2.4). Quality assessment of arrays included exploration of distributions of probe intensities across all arrays, of average background values, and RNA quality was examined by RNA degradation plots. Diagnostic plots based on a probe level model (PLM) have been used to rule out chips with spatial artifacts (Chip pseudo-images, normalized unscaled standard error (NUSE) plot and relative log expression (RLE) plot). Background adjusted normalized data was retrieved by the GCRMA (robust multi-array average) procedure.
 
Submission date Jul 16, 2010
Last update date Mar 07, 2012
Contact name Kristin Reiche
E-mail(s) kristin.reiche@izi.fraunhofer.de
Organization name Fraunhofer Institute for Cell Therapy and Immunology
Department Diagnostics
Street address Perlickstr. 1
City Leipzig
ZIP/Postal code 04103
Country Germany
 
Platform ID GPL571
Series (2)
GSE17362 miRNA expression, mRNA expression upon miRNA reconstitution, and direct mRNA target identification in prostate cancer cell lines
GSE22979 Profiling of direct mRNA targets of miR-130a, miR-203 and miR-205 in prostate cancer cell line LNCaP

Data table header descriptions
ID_REF
VALUE GCRMA normalized signal intensity

Data table
ID_REF VALUE
1007_s_at 6.67072994354932
1053_at 5.28339645481684
117_at 2.67189509759439
121_at 2.36314663447262
1255_g_at 2.34684254851049
1294_at 2.43187173173351
1316_at 2.59119307530465
1320_at 2.36198453210222
1405_i_at 5.56963723885707
1431_at 2.34684254851049
1438_at 2.55908560679822
1487_at 5.98104444832883
1494_f_at 2.34684254851049
1598_g_at 2.35794571531874
160020_at 2.36173269220801
1729_at 4.62999590087426
1773_at 2.83803025882584
177_at 2.34684254851049
179_at 2.52269694535494
1861_at 4.01659046962965

Total number of rows: 22277

Table truncated, full table size 606 Kbytes.




Supplementary file Size Download File type/resource
GSM567169.CEL.gz 1.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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