|
Status |
Public on Jun 01, 2016 |
Title |
BB10a |
Sample type |
RNA |
|
|
Source name |
Cells with high bone forming capacity in vivo
|
Organism |
Homo sapiens |
Characteristics |
cell type: Bone marrow derived stromal cells immortalized with telomerase gene treatment: No treatment basal culture condition passage: P83
|
Extracted molecule |
total RNA |
Extraction protocol |
The RNA was isolated using the RNeasy Mini Kit (Qiagen), including RNase-free Dnase (Qiagen) digestion (RNase-free DNase Set, Quiagen) has been applied on the columns during isolation.
|
Label |
biotin
|
Label protocol |
Illumina Gene Expression protocols contain a first- and second-strand reverse transcription step, followed by a single in vitro transcription (IVT) amplification that incorporates biotin-labeled nucleotides. Subsequent steps include array hybridization, washing, blocking, and streptavadin-Cy3 staining. Fluorescence emission by Cy3 is quantitatively detected for downstream analysis.
|
|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
replicate 1
|
Data processing |
The data were normalised using rank invariant normalisation after background subtraction using the Gene Expression Module 1.8.0 of GenomeStudio V2010.3 (Illumina).
|
|
|
Submission date |
May 29, 2015 |
Last update date |
Jun 01, 2016 |
Contact name |
Wasco Wruck |
E-mail(s) |
wasco.wruck@med.uni-duesseldorf.de
|
Organization name |
Universitätsklinikum Düsseldorf
|
Street address |
Moorenstr. 5
|
City |
Düsseldorf |
ZIP/Postal code |
40225 |
Country |
Germany |
|
|
Platform ID |
GPL6883 |
Series (1) |
GSE69358 |
Association between in vivo bone formation and ex vivo migration capacity of human bone marrow stromal cells |
|