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Sample GSM644204 Query DataSets for GSM644204
Status Public on Apr 01, 2012
Title Cybrid from haplogroup F, biological rep 4, technical rep 1
Sample type RNA
 
Source name Cybrid clone with mtDNA from person 4 in haplogroup F
Organism Homo sapiens
Characteristics cell type: Cybrid clone
mtdna from: person 4
mtdna haplogroup: F
Treatment protocol Cybrid clones from three mtDNA haplogroups were generated as follows. Platelets from twelve persons from three mtDNA haplogroups were separated from whole blood by centrifugation and fusion was carried out by mixing rho0 cells with platelets in a 1:1 ratio and then centrifuging at 1,500g for 15 miniutes. DMEM was removed and the cells were resuspended in 0.8 ml of 50% (v/v) polyethylene glycol (Signam-Aldrich). Sixty seconds after fusion, the cells were resuspended in DMEM and left to recover at 37 degree Celcius for 45 minutes. 24 fours after fusion, the medium was replaced with DMEM lacking uridine to select against unfused cells.
Growth protocol The rho0 cell was obtained after long-term exposure of osteoscarcoma cell line to ethidium bromide (50ng/ml) and was grown in Dulbecco's modified Eagle's medium (DMEM) supplemented with 100 mg/ml 5-bromodeoxyuridine (BrdU), 50 ug/ml uridine, and 10% fetal bovine serum (FBS).
Extracted molecule total RNA
Extraction protocol Isolation of total RNA from cells was performed using Rneasy Micro Kit (Qiagen, Valencia, CA) according to the manufacturer's instructions.
Label biotin
Label protocol Targets were prepared by using the GeneChip Whole Transcript Sense Target Labeling Assay (Affymetrix, Santa Clara, CA).
 
Hybridization protocol The prepared targets were hybridized to GeneChip Human Gene 1.0 ST Array (Affymetrix, Santa Clara, CA).
Scan protocol GeneChips were scanned using Scanner 3000 7G (Affymetrix, Santa Clara, CA) according to the manufacturer's instructions.
Description Gene expression data from cybrid clone F-4
F-4-1
Data processing The CEL files were imported to Affymetrix Expression Console software and normalized by RMA (Robust Multi-chip Average) method and log2 transformed.
 
Submission date Dec 21, 2010
Last update date Apr 01, 2012
Contact name Seungwoo Hwang
E-mail(s) [email protected]
Phone 82-42-879-8544
Organization name Korea Research Institute of Bioscience and Biotechnology
Department Korean Bioinformation Center
Street address 52 Eoeun-dong Yuseong-gu
City Daejeon
ZIP/Postal code 305-806
Country South Korea
 
Platform ID GPL6244
Series (1)
GSE26244 Expression data from cytoplasmic hybrid (cybrid) and rho0 cells

Data table header descriptions
ID_REF
VALUE RMA-processed, log2 transformed intensity

Data table
ID_REF VALUE
7896736 4.26791
7896738 2.913649
7896740 3.027108
7896742 6.951169
7896744 4.438203
7896746 7.847636
7896748 7.930996
7896750 3.833894
7896752 7.344481
7896754 4.933681
7896756 4.792456
7896759 6.749898
7896761 5.907737
7896779 6.512788
7896798 6.500009
7896817 5.913968
7896822 7.974959
7896859 5.027401
7896861 3.460606
7896863 4.915191

Total number of rows: 33297

Table truncated, full table size 549 Kbytes.




Supplementary file Size Download File type/resource
GSM644204.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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