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Sample GSM418132 Query DataSets for GSM418132
Status Public on Aug 01, 2010
Title T6(6)_leukemia_Tripz_No Dox
Sample type RNA
 
Source name T6(6) leukemic cells infected with the empty Tripz vector, no Dox, control (no Igf1r knockdown)
Organism Mus musculus
Characteristics cell type: leukemic cells derived from Gata1s mutant fetal progenitors
igf1r knockdown: no
Treatment protocol Doxycycline was or was not added to the culture medium.
Growth protocol Cells were grown in IMDM+10%FCS+IL3 or Tpo.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA followed by cleaning up using columns from the Promega SV total RNA isolation kit.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
 
Hybridization protocol The fragmented cRNA was added to a hybridization solution containing several biotinylated control oligonucleotides (for quality control), and hybridized to MOE 430.2 chips overnight at 45°C. The chips were then transferred to a fluidics instrument that performs washes to remove cRNA that had not hybridized to its complementary oligonucleotide probe. The bound cRNA was then fluorescently labeled using phycoerythrin-conjugated streptavidin (SAPE); additional fluors were then added using biotinylated anti-streptavidin antibody and additional SAPE.
Scan protocol Each cRNA bound at its complementary oligonucleotide was excited using a confocal laser scanner, and the positions and intensities of the fluorescent emissions were captured.
Description Gene expression data from T6(6) leukemic cells without Igf1r knockdown.
Data processing The raw CEL files were imported into dChip and normalized with dChip. After normalization, the model-based expression values were calculated by dChip and exported.
 
Submission date Jun 17, 2009
Last update date Jul 23, 2010
Contact name Zhe Li
E-mail(s) [email protected]
Phone 617-919-2052
Organization name Children's Hospital Boston
Department Division of Hematology/Oncology
Lab Stuart Orkin's Lab
Street address
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platform ID GPL1261
Series (2)
GSE16655 Developmental stage-specific interplay between GATA1 and IGF signaling in fetal hematopoiesis and leukemogenesis
GSE16684 Murine M7 leukemia derived from retroviral insertional mutagenesis of Gata1s fetal progenitors depends on IGF signaling

Data table header descriptions
ID_REF
VALUE dChip-normalized signal intensity

Data table
ID_REF VALUE
AFFX-BioB-5_at 340.131
AFFX-BioB-M_at 466.079
AFFX-BioB-3_at 366.51
AFFX-BioC-5_at 713.854
AFFX-BioC-3_at 803.04
AFFX-BioDn-5_at 1479.19
AFFX-BioDn-3_at 2568.83
AFFX-CreX-5_at 5930.87
AFFX-CreX-3_at 5551.93
AFFX-DapX-5_at 12.0906
AFFX-DapX-M_at 8.50316
AFFX-DapX-3_at 3.88707
AFFX-LysX-5_at 5.93554
AFFX-LysX-M_at 12.1639
AFFX-LysX-3_at 9.28847
AFFX-PheX-5_at 3.39299
AFFX-PheX-M_at 5.27383
AFFX-PheX-3_at 26.0242
AFFX-ThrX-5_at 6.90317
AFFX-ThrX-M_at 5.93787

Total number of rows: 45101

Table truncated, full table size 850 Kbytes.




Supplementary file Size Download File type/resource
GSM418132.CEL.gz 3.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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