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Sample GSM610624 Query DataSets for GSM610624
Status Public on Jun 27, 2011
Title MT2-GMP 3
Sample type RNA
 
Source name Murine granulocyte monocyte progenitor (GMP); transduced with MOZ-TIF2 oncogene
Organism Mus musculus
Characteristics strain: C57BL/6
cell type: granulocyte monocyte progenitor (GMP)
transduction protocol: transduced with MOZ-TIF2 oncogene
Extracted molecule total RNA
Extraction protocol 36 hours after spininoculation of oncogene or empty-vector transduced GMP, GFP positive cells were homogenized with TRIzol® Reagent (Invitrogen, Carlsbad, CA) according to manufacturer’s instructions. RNA isolated from the above populations along with sorted normal LSK, GMP, and MOZ-TIF2 leukemic GMP were quantitated with the Quant-iT™ RiboGreen® RNA Reagent and Kit (Invitrogen) according to manufacturer’s specifications, and used for RNA amplification and hybridization as previously published.
Label biotin
Label protocol As per the manufacturer's instructions and as previously published, with one modification: biotinylated CTP and UTP (Enzo Diagnostics, Farmingdale, NY) in a 2.5:1 proportion to non-biotinylated CTP and UTP. All RNA populations were simultaneously amplified.
 
Hybridization protocol Gene expression levels were measured using Affymetrix (Santa Clara, CA) GeneChip Mouse Genome 430A 2.0 arrays (22,690 probesets) with hybridisation and washes as per the manufacturers specifications.
Scan protocol As per Affymetrix specifications.
Description Gene expression data from murine granulocyte monocyte progenitor (GMP); transduced with MOZ-TIF2 oncogene
H_MT2 3_020407.CEL
Data processing The starting point for all analyses was the ''.CEL'' files from the MAS5 software. Data was analyzed using the R statistical package bioconductor. Data quality was assessed using functions in the affy and affyPLM packages and outlier arrays were removed from subsequent analysis.
The GCRMA algorithm (ver. 2.4.1) was used to obtain normalized expression estimates.
 
Submission date Oct 19, 2010
Last update date Jun 27, 2011
Contact name Brian J.P. Huntly
E-mail(s) [email protected]
URL http://www.cam.ac.uk/
Organization name University of Cambridge
Department Cambridge Institute for Medical Research
Lab Department of Haematology
Street address Wellcome Trust/MRC Building, Hills Road
City Cambridge
ZIP/Postal code CB2 0XY
Country United Kingdom
 
Platform ID GPL8321
Series (1)
GSE24797 Common and overlapping oncogenic pathways contribute to the evolution of acute myeloid leukemias

Data table header descriptions
ID_REF
VALUE GCRMA signal intensity

Data table
ID_REF VALUE
1415670_at 7.6164474276
1415671_at 8.3782935573
1415672_at 9.4649680404
1415673_at 9.1362156756
1415674_a_at 9.7293428414
1415675_at 8.2283550857
1415676_a_at 11.3892033597
1415677_at 7.6043325590
1415678_at 8.1324291913
1415679_at 10.8101802555
1415680_at 8.2645051153
1415681_at 9.0435555583
1415682_at 6.1204497721
1415683_at 10.8140343523
1415684_at 7.1296079651
1415685_at 7.2677899549
1415686_at 7.7803349391
1415687_a_at 11.6297066170
1415688_at 8.9574544998
1415689_s_at 6.6171099525

Total number of rows: 22690

Table truncated, full table size 547 Kbytes.




Supplementary file Size Download File type/resource
GSM610624.CEL.gz 1.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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