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Sample GSM1045338 Query DataSets for GSM1045338
Status Public on Jun 30, 2015
Title Mesenchymal stromal cell, osteosarcoma patient, sample 009
Sample type RNA
 
Source name Osteosarcoma patient MSC
Organism Homo sapiens
Characteristics cell type: Mesenchymal stromal cells
gender: male
age: 15
Growth protocol Bone marrow derived mononuclear cells were obtained from 5 to 15 ml of heparinized bone marrow aspirate by density gradient centrifugation on Ficoll. Cells were plated on non-coated 75 cm2 polystyrene flasks at a cell density of 160000/cm2 in complete culture medium (LG-DMEM [Invitrogen, Paisley, United Kingdom] supplemented with penicillin and streptomycin [merk] and 10% fetal bovine serum [FBS; HyClone, Verviers, Belgium]). We used a characterized and defined FBS batch preselected for its potential to support MSC expansion and continued to use this specific batch throughout the culture period.
Extracted molecule total RNA
Extraction protocol RNA was isolated from frozen cell pellets of at least 1*10e6 undifferentiated mesenchymal stem cells at passage 2 to 5 using TRIzol reagent (Invitrogen). Cells were lysed in TRIzol, followed by phase separation in chloroform (merk), precipitation using 2-propanolol (merk) and washing in 75% ethanol. RNA clean-up was performed using the Qiagen Rneasy mini kit with on-column DNAse treatment. RNA quality and concentration were measured using an Agilent 2100 Bioanalyzer and Nanodrop ND-1000, respectively.
Label biotin
Label protocol As per manufacturer's instructions.
 
Hybridization protocol As per manufacturer's instructions.
Scan protocol As per manufacturer's instructions.
Description Gene expression data were exported from BeadStudio version 3.1.3.0 (Illumina) in GeneSpring probe profile format. Two supplementary/raw data files are present because each array that represents one Sample consists of 2 chips. The supplementary/raw data files represent the bead level data (2 raw .txt files per sample, containing all intensities per bead).
Data processing Microarray data were normalized using the Cubic Spline normalization method with the Illumina BeadStudio Gene Expression Module (Illumina). Statistical analysis of microarray was performed using Significance Analysis for Microarrays (SAM)
 
Submission date Nov 28, 2012
Last update date Jul 01, 2015
Contact name Marieke Lydia Kuijjer
Organization name Centre for Molecular Medicine Norway
Lab Kuijjer
Street address Gaustadalléen 21
City Oslo
ZIP/Postal code 0349
Country Norway
 
Platform ID GPL13376
Series (1)
GSE42572 Gene expression analysis of mesenchymal stromal cells obtained from healthy donors and osteosarcoma patients

Data table header descriptions
ID_REF
VALUE Normalized intensity

Data table
ID_REF VALUE
ILMN_1681101 86.48296
ILMN_1671854 75.19705
ILMN_1659893 92.36398
ILMN_1669592 110.6592
ILMN_1703142 567.4702
ILMN_1676737 101.5972
ILMN_1740252 1768.566
ILMN_1747665 79.29193
ILMN_1655796 117.2456
ILMN_1699644 105.5646
ILMN_1735038 94.67353
ILMN_1659953 90.66132
ILMN_1746673 82.86719
ILMN_1789991 260.8604
ILMN_1763444 91.97129
ILMN_1776157 284.4896
ILMN_1778079 84.41752
ILMN_1702764 180.3416
ILMN_1674893 89.9954
ILMN_1688067 91.19382

Total number of rows: 48701

Table truncated, full table size 1040 Kbytes.




Supplementary file Size Download File type/resource
GSM1045338_1674120172_E_1.txt.gz 11.1 Mb (ftp)(http) TXT
GSM1045338_1674120172_E_2.txt.gz 11.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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