NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM617221 Query DataSets for GSM617221
Status Public on Nov 18, 2010
Title 1 PPARg +/-LysCre IL-4 macrophage
Sample type RNA
 
Source name PPARg +/-LysCre bone marrow-derived macrophage treated with IL-4
Organism Mus musculus
Characteristics mouse: 1
strain: C57Bl/6
genotype/variation: PPARg +/-LysCre
cell type: bone marrow-derived alternatively activated macrophage
treatment: Control
time: 9 days
Treatment protocol Cell were treated after plating into 6-well cell culture plates with the indicated cytokines and vehicle (DMSO:ethanol) or 1 uM Rosiglitazone.
Growth protocol Bone marrow cells were isolated from the femur, washed twice with PBS and cultured in RPMI+10% FCS supplemented with glutamine, penicillin and streptomycin and 20 ng/ml M-CSF+20 ng/ml IL-4 for macrophage or 20 ng/ml GM-CSF+20 ng/ml IL-4 for iDC differentiation. Fresh media and cytokines were added every other day for 9 days.
Extracted molecule total RNA
Extraction protocol Qiagen extraction of total RNA was performed according to the manufacturer's instructions.
Label DIG
Label protocol 1 ug of total RNA was used to transcribe DIG-labeled cRNA using Applied Biosystems Chemiluminescent RT-IVT Kit V2.0.
 
Hybridization protocol Microarray hybridization (using twenty micrograms of fragmented, DIG-labeled cRNA) and processing were performed according to Applied Biosystems protocols.
Scan protocol Chemiluminescence detection, imaging, auto gridding, and image analysis was done according to Applied Biosystems protocols and the 1700 Chemiluminescent Microarray Analyzer Software v. 1.0.3.
Description Gene expression data of IL-4-treated bone marrow-derived macrophages derived from PPARg +/-LysCre mouse
Data Sample 1.txt
Data processing The data were generated with ABI1700 and txt files were further analyzed in GeneSpring 7.3.
 
Submission date Nov 03, 2010
Last update date Nov 18, 2010
Contact name Attila Szanto
E-mail(s) attila.szanto@gmail.com
Organization name Massachusetts General Hospital
Department Molecular Biology
Lab Lee Lab
Street address 185 Cambridge St.
City Boston
State/province MA
ZIP/Postal code 02446
Country USA
 
Platform ID GPL2995
Series (2)
GSE16387 Licensing of PPARg-regulated gene expression by IL-4-induced alternative macrophage activation
GSE25125 PPARg and IL-4-induced gene expression data from PPARg +/- LysCre and PPARg fl/- LysCre mouse bone marrow-derived alternatively activated macrophages and immature dendritic cells (iDCs)

Data table header descriptions
ID_REF
VALUE Normalized signal intensity after per chip normalization and per gene normalization.

Data table
ID_REF VALUE
370264 0.7683409
577485 1.5760363
456277 2.5626793
422129 1.3065786
312133 0.59450513
828031 0.97644156
624353 1.220317
774404 1.8276905
301015 0.7737035
371879 0.91700774
388961 1.2591803
892920 1.2910204
498201 0.7478268
388093 1.7923855
787300 1.2137921
470796 0.5541478
437610 1.0017158
466290 0.9990016
329956 0.60832316
397784 0.7499427

Total number of rows: 33012

Table truncated, full table size 551 Kbytes.




Supplementary file Size Download File type/resource
GSM617221.txt.gz 879.1 Kb (ftp)(http) TXT
Processed data included within Sample table

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