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Sample GSM434411 Query DataSets for GSM434411
Status Public on Aug 24, 2009
Title pKLO beta-catenin shRNA,, biological rep1
Sample type RNA
 
Source name Cultured MM1S cell line, treated (maternal transcripts)
Organism Homo sapiens
Characteristics cell line: Multiple myeloma line MM1.S
protocol: beta-catenin knockdown
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 6.628011915
1053_at 6.438161684
117_at 6.240420332
121_at 8.209476584
1255_g_at 6.336979612
1294_at 6.98763535
1316_at 7.100054178
1320_at 5.514987414
1405_i_at 7.460457052
1431_at 5.40638735
1438_at 5.241556127
1487_at 6.858673595
1494_f_at 6.400919391
1552256_a_at 7.423213669
1552257_a_at 7.957513707
1552258_at 5.275000511
1552261_at 7.006131952
1552263_at 5.714518119
1552264_a_at 6.62090193
1552266_at 5.448839959

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM434411.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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