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Sample GSM709685 Query DataSets for GSM709685
Status Public on Apr 16, 2011
Title Non-phosphorylated FTY720 induces apoptosis of human microglia by activating SREBP2(#4)
Sample type RNA
 
Source name HMO6 human microglia treated with FTY720 dissolved in ETOH for 2 hours
Organism Homo sapiens
Characteristics cells: HMO6 microglia
tissue: Brain
Biomaterial provider Seung U. Kim, Division of Neurology, Department of Medicine, University of British Columbia Hospital, University of British Columbia, Vancouver, British Columbia, Canada
Treatment protocol HMO6 cells were exposed for 2 hours to 10 microM non-phosphorylated FTY720 (Calbiochem) or an equal amount of vehicle (ETOH).
Growth protocol The cells were maintained in Dulbecco's Modified Eagle's medium (DMEM; Invitrogen, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS), 100 U/ml penicillin and 100 microgram/ml streptomycin (feeding medium).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from the cells by using the TRIZOL Plus RNA Purification kit (Invitrogen). The quality of total RNA was evaluated on Agilent 2100 Bioanalyzer (Agilent Technologies).
Label biotin
Label protocol One hundred ng of total RNA was processed for cRNA synthesis, fragmentation, and terminal labeling with the GeneChip Whole Transcript Sense Target Labeling and Control Reagents (Affymetrix)
 
Hybridization protocol Hybridization was performed at 45℃ for 17 hours. The arrays were washed and stained in the GeneChip Fluidic Station 450 (Affymetrix) by using Hybridization, Wash and Stain kit (Affymetrix).
Scan protocol The arrays were scanned by the GeneChip Scanner 3000 7G (Affymetrix).
Description The HMO6 cell line was established by immortalizing cultured microglia isolated from human embryonic telencephalon tissues with a retroviral vector PASK1.2 encoding v-myc oncogene. HMO6 cells express the markers of the microglia/macrophage lineage cells, including CD11b, CD68, CD86, HLA-ABC, HLA-DR, and ricinus communis agglutinin lectin-1 (RCA), serving as a model of human microglia both in vitro and in vivo.
Data processing The data expressed as CEL files were normalized by the robust multiarray average (RMA) method with the Expression Console software version 1.1 (Affymetrix).
 
Submission date Apr 15, 2011
Last update date Apr 16, 2011
Contact name Jun-ichi Satoh
E-mail(s) [email protected]
Organization name Meiji Pharmaceutical University
Department Bioinformatics
Lab Molecular Neuropathology
Street address 2-522-1 Noshio, Kiyose
City Tokyo
ZIP/Postal code 204-8588
Country Japan
 
Platform ID GPL6244
Series (1)
GSE28642 Non-phosphorylated FTY720 induces apoptosis of human microglia by activating SREBP2

Data table header descriptions
ID_REF
VALUE RMA normalized signal intensity

Data table
ID_REF VALUE
7892501 8.08212
7892502 5.1273
7892503 3.70492
7892504 9.78246
7892505 3.60438
7892506 3.85123
7892507 5.27237
7892508 5.47979
7892509 13.0488
7892510 4.4984
7892511 2.19885
7892512 6.46489
7892513 4.77937
7892514 11.5896
7892515 8.83577
7892516 7.24584
7892517 6.06947
7892518 2.68745
7892519 5.69617
7892520 9.44723

Total number of rows: 33297

Table truncated, full table size 516 Kbytes.




Supplementary file Size Download File type/resource
GSM709685.CEL.gz 4.1 Mb (ftp)(http) CEL
GSM709685.chp.gz 255.9 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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