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Sample GSM610630 Query DataSets for GSM610630
Status Public on Jun 27, 2011
Title AE-GMP 2
Sample type RNA
 
Source name Murine granulocyte monocyte progenitor (GMP); transduced with AML1-ETO oncogene
Organism Mus musculus
Characteristics strain: C57BL/6
cell type: granulocyte monocyte progenitor (GMP)
transduction protocol: transduced with AML1-ETO 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 AML1-ETO oncogene
L_AE 2_062007.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 7.6956113727
1415671_at 9.0846563885
1415672_at 9.5689590061
1415673_at 8.2860375676
1415674_a_at 9.8509833306
1415675_at 8.3369150950
1415676_a_at 11.0825697392
1415677_at 8.3964689666
1415678_at 8.3671093804
1415679_at 11.3020482826
1415680_at 8.5207509672
1415681_at 9.3342496879
1415682_at 5.8226838376
1415683_at 11.0622431961
1415684_at 7.6231864067
1415685_at 7.4237017083
1415686_at 7.7551914906
1415687_a_at 11.7502653896
1415688_at 9.1720742494
1415689_s_at 7.2250806396

Total number of rows: 22690

Table truncated, full table size 547 Kbytes.




Supplementary file Size Download File type/resource
GSM610630.CEL.gz 2.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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