NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1260352 Query DataSets for GSM1260352
Status Public on Nov 07, 2013
Title LNCaP.872.DMSO.rep3
Sample type RNA
 
Source name LNCaP.872, DMSO control/16h, rep3
Organism Homo sapiens
Characteristics cell line type: prostate cancer cell line
cell line: LNCap
treatment: sh872, DMSO control/16h
Treatment protocol shRNA expression was performed for 4 days. Coumpound treatment was 20 µM for 16 hours. Final DMSO concentration (treatment and control) was at 0.2%.
Growth protocol Cells were grown in RPMI media supplemented with 10% FBS
Extracted molecule total RNA
Extraction protocol QIAgen kit according to manufacturer protocol
Total RNA from the samples was normalized to 50 ng/ul and the GeneChip® 3’ IVT Express Kit (Affymetrix PN 901253) was used for amplification according to the standard protocol. The total RNA underwent reverse transcription to synthesize first-strand cDNA. This cDNA was then converted into a double-stranded DNA template for transcription. In vitro transcription synthesized aRNA and incorporated a biotin-conjugated nucleotide. The aRNA was then purified to remove unincorporated NTPs, salts, enzymes, and inorganic phosphate. Fragmentation of the biotin-labeled aRNA prepared the samples for hybridization to Affymetrix HT-HG U133 A peg arrays (Affymetrix PN 900751). 
Label biotin
Label protocol Labeling was conducted manually, using the Affymetrix 3' IVT Express Kit (Affymetrix PN 901253) according to the attached standard protocol. Reactions were cycled on the Thermo Hybaid MBS Satellite 0.2G cycler. http://www.affymetrix.com/estore/esearch/search.jsp?pd=131549&N=429496729
 
Hybridization protocol Hybridization and scanning were conducted using the Affymetrix GeneTitan (MC) instrument (Affymetrix PN 00-0372), according to the attached standard protocol.http://www.affymetrix.com/estore/esearch/search.jsp?Ntt=titan&basic=1
Scan protocol CEL files were produced using the Affymetrix GeneChip Command Console software (Affymetrix PN agcc01) integrated with the GeneTitan. http://www.affymetrix.com/estore/browse/products.jsp?productId=131429#1_1
Data processing The data were analyzed with R 3.0.2, using the package affy_1.40.0, and RMA as normalization method. RMA was used with default options (normalize=TRUE, background=TRUE) and with the package hthgu133ahsentrezgcdf v17.1.0 from Brainarray for the CDF file.
 
Submission date Nov 06, 2013
Last update date Nov 07, 2013
Contact name Marius Pop
E-mail(s) [email protected]
Organization name DFCI
Street address 450 Brookline ave
City Boston
ZIP/Postal code 02215
Country USA
 
Platform ID GPL17897
Series (1)
GSE52154 Gene expression signature overlap between shETV1 and BRD32048 in LNCaP and SK-MEL-28

Data table header descriptions
ID_REF
VALUE log2 RMA signal

Data table
ID_REF VALUE
10_at 3.568876402
100_at 6.395968408
1000_at 3.4223108
10000_at 3.144352187
10001_at 8.071932525
10002_at 2.999125663
10003_at 4.758447801
10004_at 3.102987107
100048912_at 3.130425789
10005_at 7.05795444
10006_at 7.736132339
10007_at 8.570282757
10009_at 2.922325344
100093698_at 3.407248852
1001_at 3.608064847
10010_at 6.843835304
100126791_at 2.920067349
100128124_at 3.429613684
100128640_at 3.31687591
100129128_at 3.350712995

Total number of rows: 12092

Table truncated, full table size 241 Kbytes.




Supplementary file Size Download File type/resource
GSM1260352_FORKS_p_Pop_24Affy133AHT_001_HT_HG-U133A_24-HTA_F05_783078.CEL.gz 2.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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