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Status |
Public on Aug 01, 2010 |
Title |
T6(6)_leukemia_Tripz_No Dox |
Sample type |
RNA |
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Source name |
T6(6) leukemic cells infected with the empty Tripz vector, no Dox, control (no Igf1r knockdown)
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Organism |
Mus musculus |
Characteristics |
cell type: leukemic cells derived from Gata1s mutant fetal progenitors igf1r knockdown: no
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Treatment protocol |
Doxycycline was or was not added to the culture medium.
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Growth protocol |
Cells were grown in IMDM+10%FCS+IL3 or Tpo.
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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.
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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.
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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.
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Description |
Gene expression data from T6(6) leukemic cells without Igf1r knockdown.
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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.
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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 |
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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 |
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