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Sample GSM709684 Query DataSets for GSM709684
Status Public on Apr 16, 2011
Title Non-phosphorylated FTY720 induces apoptosis of human microglia by activating SREBP2(#3)
Sample type RNA
 
Source name HMO6 human microglia treated with ethanol 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 7.55907
7892502 4.51395
7892503 2.85883
7892504 9.82112
7892505 2.99716
7892506 5.28554
7892507 5.09165
7892508 5.05379
7892509 12.8939
7892510 5.33589
7892511 2.07957
7892512 6.97943
7892513 3.72832
7892514 11.4937
7892515 9.0019
7892516 7.4
7892517 6.25019
7892518 2.5321
7892519 5.77758
7892520 9.35043

Total number of rows: 33297

Table truncated, full table size 516 Kbytes.




Supplementary file Size Download File type/resource
GSM709684.CEL.gz 4.1 Mb (ftp)(http) CEL
GSM709684.chp.gz 255.9 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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