NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1045335 Query DataSets for GSM1045335
Status Public on Jun 30, 2015
Title Mesenchymal stromal cell, osteosarcoma patient, sample 004
Sample type RNA
 
Source name Osteosarcoma patient MSC
Organism Homo sapiens
Characteristics cell type: Mesenchymal stromal cells
gender: female
age: 14
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 83.88202
ILMN_1671854 80.52278
ILMN_1659893 92.55672
ILMN_1669592 97.28108
ILMN_1703142 232.6346
ILMN_1676737 97.40863
ILMN_1740252 1296.13
ILMN_1747665 78.36105
ILMN_1655796 338.7847
ILMN_1699644 262.0117
ILMN_1735038 171.6406
ILMN_1659953 108.9271
ILMN_1746673 113.6523
ILMN_1789991 824.6251
ILMN_1763444 93.28206
ILMN_1776157 265.3347
ILMN_1778079 93.61118
ILMN_1702764 218.9996
ILMN_1674893 99.7191
ILMN_1688067 90.15685

Total number of rows: 48701

Table truncated, full table size 1041 Kbytes.




Supplementary file Size Download File type/resource
GSM1045335_1674120172_D_1.txt.gz 11.1 Mb (ftp)(http) TXT
GSM1045335_1674120172_D_2.txt.gz 11.1 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap