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Sample GSM1910847 Query DataSets for GSM1910847
Status Public on Jan 24, 2017
Title corneal_endothelium_control_A31
Sample type RNA
 
Source name corneal endothelium control
Organism Homo sapiens
Characteristics rna integrity number: 7.70
gender: male
age: 26 years
tissue: corneal endothelium with Descemet's membrane
group: donor cornea as normal control
number of cells per mm²: 2300
Cause of death: trauma
Biomaterial provider University Hospitals Leuven (Belgium), Department of Ophthalmology
Treatment protocol The sample was collected in RNAlater.
Growth protocol The donor cornea was provided in storage medium.
Extracted molecule total RNA
Extraction protocol Tissues were disrupted and homogenized manually with a Disposable Pestle (VWRTM International, Radnor, Pennsylvania). RNA extraction was performed with RNeasy® Micro Kit (Qiagen), without DNase treatment.
Label biotin
Label protocol RNA concentration and purity were determined spectrophotometrically using the Nanodrop ND-1000 (Nanodrop Technologies) and RNA integrity was assessed using a Bioanalyser 2100 (Agilent). Using the Ambion WT Expression Kit, per sample, an amount of 100 ng of total RNA spiked with bacterial poly-A RNA positive controls (Affymetrix) was converted to double stranded cDNA in a reverse transcription reaction. Next the sample was converted and amplified to antisense cRNA in an in vitro transcription reaction which was subsequently converted to single stranded sense cDNA. Finally, samples were fragmented and labeled with biotin in a terminal labeling reaction according to the Affymetrix WT Terminal Labeling Kit.
 
Hybridization protocol A mixture of fragmented biotinylated cDNA and hybridisation controls (Affymetrix) was hybridised on Affymetrix GeneChip Human Gene 1.0 ST Arrays followed by staining and washing in a GeneChip® fluidics station 450 (Affymetrix) according to the manufacturer’s procedures.
Scan protocol To assess the raw probe signal intensities, chips were scanned using a GeneChip® scanner 3000 (Affymetrix).
Description corneal endothelium control
Data processing Data were processed with RMA (as implemented in the XPS package of Bioconductor). Reported values are on log2-scale.
 
Submission date Oct 19, 2015
Last update date Jan 24, 2017
Contact name Joost J van den Oord
E-mail(s) joost.vandenoord@med.kuleuven.be
Phone +32 16 33 65 91
Organization name KU Leuven
Department Department of Imaging & Pathology
Lab Translational Cell & Tissue Research
Street address Minderbroedersstraat 12, block q, box 1032
City Leuven
ZIP/Postal code 3000
Country Belgium
 
Platform ID GPL6244
Series (2)
GSE74123 Identification of Circulating Fibrocytes and Dendritic Derivatives in Corneal Endothelium of Patients with Fuchs' Dystrophy [microarray expression analysis]
GSE75676 Identification of Circulating Fibrocytes and Dendritic Derivatives in Corneal Endothelium of Patients with Fuchs' Dystrophy

Data table header descriptions
ID_REF
VALUE log2 RMA

Data table
ID_REF VALUE
7892796 13.1391580109058
7892925 10.0920171075408
7893130 11.5413386579708
7893306 7.97056034707536
7893613 9.2838685404703
7893939 9.01704500393812
7894584 5.30885594117364
7894611 7.49042572536166
7894970 13.4741495484973
7895139 6.60055373235313
7895220 10.4955752528005
7896160 9.8130083409023
7896366 12.4754066600082
7896687 6.9721297093383
7896688 5.32378797212704
7896689 6.08438109550497
7896690 6.10475598696226
7896691 6.40780649643233
7896692 7.53675231340094
7896693 4.29900282050038

Total number of rows: 28886

Table truncated, full table size 702 Kbytes.




Supplementary file Size Download File type/resource
GSM1910847_hyb8268.CEL.gz 4.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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