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Sample GSM839160 Query DataSets for GSM839160
Status Public on Apr 05, 2013
Title fibroblast_patient_GIO_2_1
Sample type RNA
 
Source name human fibroblast, Q10 deficient patient GIO
Organism Homo sapiens
Characteristics patient: chromosome 9 deletion containg COQ4 gene, CoQ10 deficiency
gender: boy
age: unknown
treatment: none
Treatment protocol Coenzyme Q10 pre-diluted in FBS was added to the plates at a final concentration of 30 micromolar (Coenzyme Q10, Synthetic Minimun 98%, HPLC, Sigma).
Growth protocol Control fibroblasts and those from Q-deficient patients were cultured at 37°C using DMEM 1 g/L Glucose, L-Glutamine, Pyruvate (Invitrogen, Prat de Llobregat, Barcelona) supplemented with an antibiotic/antimycotic solution (Sigma Chemical Co., St. Louis, Missouri) and 20% fetal bovine serum (FBS, Linus).
Extracted molecule total RNA
Extraction protocol Cells were homogenized in 1 ml of Tripure Isolation Reagent (Roche) and RNA was extracted with chloroform and precipitated with 2-propanol by centrifugation at 12000 g for 10 min at 4C. After washing with 75% EtOH, RNA was resuspended in DEPC-treated water and treated with deoxiribonuclease I (Sigma) for removal of possible DNA contamination. Afterwards, RNA was cleaned using the RNeasy MinElute Cleanup kit (Qiagen), its concentration and purity were checked spectrophotometrically and its quality was verified electrophoretically. RNA was stored at –20C in RNase-free water.
Label biotin
Label protocol A cRNA probe was synthesized and fragmented from each RNA sample using Affymetrix protocols and kits provided by Qiagen.
 
Hybridization protocol Each cRNA probe was hybridized to independent GeneChip Human Genome U133 Plus 2.0 Array (Affymetrix). Hybridization was performed overnight in the GeneChip Hybridization Oven 640 at 45C with shaking at 60 rpm; washes and staining of the probe were performed in the GeneChip fluidics station using buffers and protocols provided by the manufacturer. The full system was controlled by the GeneChip Operating Software (GCOS), and both the equipment and the software were provided by Affymetrix.
Scan protocol High-quality scan of the arrays was performed with the GeneChip Scanner 3000. The full system was controlled by the GeneChip Operating Software (GCOS), and both the equipment and the software were provided by Affymetrix.
Description rep. 2, cRNA 1
unpublished data
Data processing Data extraction, cell intensity calculation and computational analysis were performed using GCOS and Expression Console Release Software from Affymetrix. The signal value was obtained using PLIER and RMA algorithms at linear scale.
 
Submission date Nov 24, 2011
Last update date Apr 05, 2013
Contact name Daniel Jose Moreno Fernandez-Ayala
E-mail(s) [email protected]
Organization name Universidad Pablo de Olavide
Lab CABD/CSIC-UPO
Street address Carretera de Utrera, Km. 1
City Sevilla
ZIP/Postal code 41013
Country Spain
 
Platform ID GPL6244
Series (2)
GSE33940 Gene expression in the mitochondrial syndrome of coenzyme Q deficiency
GSE33941 Survival transcriptome in coenzyme Q deficiency syndrome

Data table header descriptions
ID_REF
VALUE normalized signal intensities

Data table
ID_REF VALUE
7892501 22.8966
7892502 45.3824
7892503 4.41144
7892504 1101.84
7892505 9.32547
7892506 11.3249
7892507 2.54654
7892508 13.5656
7892509 2922.61
7892510 11.0529
7892511 12.5543
7892512 224.835
7892513 10.2885
7892514 1577.44
7892515 879.051
7892516 56.2548
7892517 29.1797
7892518 0.00207723
7892519 155.342
7892520 727.304

Total number of rows: 33297

Table truncated, full table size 518 Kbytes.




Supplementary file Size Download File type/resource
GSM839160_GIO21.CEL.gz 3.9 Mb (ftp)(http) CEL
GSM839160_GIO21.chp.gz 263.1 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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