NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1583300 Query DataSets for GSM1583300
Status Public on May 13, 2015
Title EML1 infected with the empty pWPI lentiviral vector - rep 2
Sample type RNA
 
Source name EML1 hematopoietic progenitor cell line
Organism Mus musculus
Characteristics cell line: EML1
treatment: empty pWPI lentiviral vector
Growth protocol EML1 cells were grown in IMDM (Iscove Modified Dulbecco’s Medium) supplemented with 20% heat-inactivated horse serum and 15% BHK/MKL cell-conditioned medium. For B-cell differentiation, OP9 stromal cells were plated in 6-well plates in Alpha Minimum Essential Medium (α-MEM) with 20% of fetal bovine serum. When they reached confluency, 50 000 EML1 cells were plated on top of the stromal cells in their specific culture medium plus supplements (IL7 10 ng/ml; FLT3L 80 ng/ml; β-mercaptoethanol, 50 μM).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using TRIzol Reagent (Gibco), followed by clean up on RNeasy mini/midi columns (RNeasy Mini/Midi Kit, Qiagen).
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA The size and the accuracy of quantitation of targets were checked by agarose gel electrophoresis of 2ug aliquots, prior to and after fragmentation. After fragmentation, targets were diluted in hybridisation buffer at a concentration of 150ug/ml.
 
Hybridization protocol Following fragmentation, 12.5 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse Gene 1.0 ST Arrays. GeneChips were washed and stained in the Affymetrix Fluidics Station.
Scan protocol Images were scanned using an Affymetrix GeneArray Scanner, using default parameters.
Description EML1 cell line: Bone marrow cells of male BDF1 mice infected with the retroviral vector LRARalpha403SN. They can be induced with IL-7 and bone marrow stromal cells to express characteristics of pre-pro-B lymphocytes.
Data processing standard Affymetrix protocol
 
Submission date Jan 13, 2015
Last update date May 14, 2015
Contact name Myriam Alcalay
E-mail(s) myriam.alcalay@ieo.eu
Organization name European Institute of Oncology
Department Experimental Oncology
Lab Functional Genomics
Street address Via Adamello 16
City Milan
ZIP/Postal code 20139
Country Italy
 
Platform ID GPL11533
Series (1)
GSE64919 Genes regulated in EML1 cells expressing the TEL-AML1 oncogene after 5 and 7 days of treatment with IL7 and FLT3 ligand.

Data table header descriptions
ID_REF
VALUE normalized signal

Data table
ID_REF VALUE
10605884 49.7315
10411593 78.1511
10351644 658.452
10461553 52.0424
10436128 49.3856
10411595 276.124
10485979 40.5089
10545940 482.491
10521515 58.8707
10486081 51.8667
10595900 345.595
10485982 73.8087
10606001 493.932
10461558 55.4741
10411609 356.577
10595892 44.3979
10571467 50.1798
10411611 179.79
10595895 53.3266
10546047 58.9322

Total number of rows: 35556

Table truncated, full table size 585 Kbytes.




Supplementary file Size Download File type/resource
GSM1583300_EML-ev_B0_B.cel.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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