NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM324786 Query DataSets for GSM324786
Status Public on Oct 27, 2008
Title Control 2
Sample type RNA
 
Source name Control
Organism Mus musculus
Characteristics nonmalignant T cells
Extracted molecule total RNA
Extraction protocol Sorted cells were homogenized for RNA isolation using the TRIZOL reagent (Invitrogen) and purified using Qiagen RNeasy minicolumns.
Label biotin
Label protocol The RNA is converted into cDNA, then double-stranded cDNA is amplified and labeled with biotinylated nucleotides by in vitro transcription to produce biotinylated complementary RNA, the cRNA is purified from the in vitro transcription reaction mixture using the RNeasy system (Qiagen).
 
Hybridization protocol Purified cRNA is processed for hybridization on the Mouse Expression-Array-430.2.0 Genechip (Affymetrix, Santa Clara) overnight at 45°C by the Microarray Core Facility of the Dana-Farber Cancer Institute. The bound cRNA is then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors are then added using biotinylated anti-streptavidin antibody and additional SAPE.
Scan protocol Each cRNA bound at its complementary oligonucleotide is excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions are captured.
Description standard processing performed by Microarray Core of DFCI
Data processing Data were loaded onto the DNA-Chip Analyzer (dChip, http://www.dchip.org) program for normalization and quantification. Normalization was performed using the default settings of the dChip software, genes were selected for expression differences higher than 1.5-fold by t test (P< 0.05) or for significant changes (P < 0.05).
 
Submission date Sep 26, 2008
Last update date Aug 28, 2018
Contact name Alexei Protopopov
Organization name UT MD Anderson Cancer Center
Department IACS
Street address 1901 East Rd
City Houston
State/province TX
ZIP/Postal code 77054
Country USA
 
Platform ID GPL1261
Series (1)
GSE12948 Oncogenesis of T-ALL and non-malignant consequences of overexpressing NOTCH1
Relations
Reanalyzed by GSE41385
Reanalyzed by GSE119085

Data table header descriptions
ID_REF
VALUE normalized signal

Data table
ID_REF VALUE
AFFX-BioB-5_at 6.91518
AFFX-BioB-M_at 7.72579
AFFX-BioB-3_at 7.18512
AFFX-BioC-5_at 9.01201
AFFX-BioC-3_at 8.94304
AFFX-BioDn-5_at 9.93741
AFFX-BioDn-3_at 11.7236
AFFX-CreX-5_at 12.7655
AFFX-CreX-3_at 12.9979
AFFX-DapX-5_at 3.42857
AFFX-DapX-M_at 3.52927
AFFX-DapX-3_at 3.45489
AFFX-LysX-5_at 3.24047
AFFX-LysX-M_at 3.59508
AFFX-LysX-3_at 3.42994
AFFX-PheX-5_at 3.54862
AFFX-PheX-M_at 3.34036
AFFX-PheX-3_at 5.69202
AFFX-ThrX-5_at 4.58653
AFFX-ThrX-M_at 3.17418

Total number of rows: 45101

Table truncated, full table size 849 Kbytes.




Supplementary file Size Download File type/resource
GSM324786.CEL.gz 6.2 Mb (ftp)(http) CEL
GSM324786.chp.gz 307.6 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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