NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM434409 Query DataSets for GSM434409
Status Public on Aug 24, 2009
Title pKLO GFP control, biological rep2
Sample type RNA
 
Source name Cultured MM1S cell line, treated (maternal transcripts)
Organism Homo sapiens
Characteristics cell line: Multiple myeloma line MM1.S
protocol: control
Treatment protocol 5x10^6 MM1.S cells lentivirally infected with control shRNA or beta-catenin shRNA vectors and sorted for GFP positive populations were cultured in triplicate, washed in PBS and then resuspended in Trizol reagent (invitrogen).
Growth protocol Cell were grown and maintained in a 37oC incubator with 5% CO2.
Extracted molecule total RNA
Extraction protocol RNA was extracted according to the manufacturer's protocol, purified using RNeasy kit (Qiagen)
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description Gene expression data from embryos younger than nuclear cycle 9, i.e. before zygotic genome activation.
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 100. Data were further process by the PLIER method.
 
Submission date Jul 28, 2009
Last update date Aug 28, 2018
Contact name Daniel Ruben Carrasco
E-mail(s) [email protected]
Organization name Dana-Farber Cancer Institute
Department Medical Oncology
Lab Carrasco
Street address 44 Binney St
City Boston
State/province MA
ZIP/Postal code MA 02115
Country USA
 
Platform ID GPL570
Series (1)
GSE17385 Gene expression profiling from MM1.S cells with control or beta-catenin knockdown.
Relations
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE normalized signal by PLIER method

Data table
ID_REF VALUE
1007_s_at 6.508035466
1053_at 7.029262219
117_at 4.984570533
121_at 8.225046431
1255_g_at 6.648846295
1294_at 6.914690174
1316_at 6.75881193
1320_at 5.334924829
1405_i_at 4.68928542
1431_at 5.233202295
1438_at 5.177310986
1487_at 6.661017002
1494_f_at 6.30668757
1552256_a_at 7.911743567
1552257_a_at 8.531161174
1552258_at 5.325488759
1552261_at 7.232269707
1552263_at 6.248353101
1552264_a_at 7.017121623
1552266_at 5.193065885

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM434409.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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