NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM363605 Query DataSets for GSM363605
Status Public on Nov 02, 2009
Title hMSC_1_1 II
Sample type RNA
 
Source name Bone marrow aspirate purified hMSCs
Organism Homo sapiens
Characteristics cell type: Bone marrow aspirate purified hMSCs
Treatment protocol None
Growth protocol Bone marrow hMSC were cultured in DMEM-LG plus Glutamax supplemented with 17% Hyclone FBS (Thermo Fisher Scientific, Waltham, MA) at 5% CO2.
Extracted molecule total RNA
Extraction protocol Frozen Liposarcoma tissue was disrupted using a Hybaid Ribolyser at a setting of 5.5 for 5 x 10 second pulses with 30 second pauses in between and RNA was extracted using the RNeasy Lipid kit (Qiagen Inc, Hilden, Germany) as per manufacturers’ instructions. Primary hMSC aspirates were isolated by centrifugation at 700 g for 15 min at 4 °C over a Ficoll-Hypaque gradient (Sigma) and total RNA was extracted using Nucleospin II RNA extraction kit (Macherey-Nagel) as per manufacutor's instructions.
Label Cy3
Label protocol 800 ng of total RNA was labelled with Cy3 using the Low RNA Input Linear Amplification Kit (Agilent technologies) as per manufacturor's instructions.
 
Hybridization protocol 100ul of purified labelled total RNA was hybridised to Agilent 4x44K whole human genome arrays for 17 hours at 65C rotating at 10 rpm and washed as as per manufacturor's instructions for one colour arrays (Agilent Technologies).
Scan protocol Slides were scanned using DNA microarray scanner model G2539A (Agilent Technologies) and Agilent Scan Control Software. Spot intensity and identity information was extracted using Agilent Feature Extraction Software.
Data processing Normalised to the 75th percentile with intensities below 0.01 being set to 0.01. Data filtered to contain only those probes with Present, Marginal or Unknown status in 22 of 26 samples.
 
Submission date Jan 23, 2009
Last update date Mar 23, 2012
Contact name W. Nicol Keith
E-mail(s) n.keith@beatson.gla.ac.uk
Organization name The University of Glasgow
Street address Center for Oncology and Applied Pharmacology, University of Glasgow, CRUK Beatson Laboratories, Garscube Estate, Switchback Road
City Glasgow
State/province Lanarkshire
ZIP/Postal code G61 1BD
Country United Kingdom
 
Platform ID GPL6480
Series (2)
GSE14529 A gene expression signature classifying telomerase and ALT immortalization II
GSE14533 A gene expression signature classifying telomerase and ALT immortalization

Data table header descriptions
ID_REF
VALUE Genespring 7.3.1 signal intensity normalised to the 75th percentile

Data table
ID_REF VALUE
A_23_P208835 6.1666355
A_32_P30187 7.2127676
A_24_P226867 2.023494
A_23_P60472 1.0211511
A_23_P98057 0.56504726
A_24_P110591 15.349877
A_23_P105044 3.09658
A_24_P664992 0.082659416
A_23_P129174 0.5961456
A_23_P103442 3.1468377
A_32_P213103 0.04217134
A_23_P31109 7.6936975
A_23_P250283 6.37761
A_23_P93562 0.4069926
A_23_P132260 0.81926876
A_23_P400465 21.553143
A_23_P5551 38.53567
A_23_P153489 5.636701
A_23_P151321 52.90386
A_23_P122906 3.3920667

Total number of rows: 24410

Table truncated, full table size 538 Kbytes.




Supplementary file Size Download File type/resource
GSM363605.txt.gz 1.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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