|
Status |
Public on Dec 19, 2008 |
Title |
SG-108A_phenotype of EPC colony assay |
Sample type |
RNA |
|
|
Source name |
cultured EPC, baseline
|
Organism |
Homo sapiens |
Characteristics |
baseline
|
Treatment protocol |
cells were harvested after 5 days.
|
Growth protocol |
Blood was collected into CPT tubes with Ficoll and sodium heparin for isolation of mononuclear cells, washed twice in PBS with 5% fetal bovine serum and re-suspended in media for endothelial progenitor-colony-forming assay.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from cultured EPC with an RNAqueous micro RNA isolation kit (Ambion, Austin, TX). Cells were lysed in buffer containing guanidinium thiocyanate.
|
Label |
biotin
|
Label protocol |
Biotin labeled with Affymetrix's IVT labeling kits (Affymetrix, Santa Clara, CA).
|
|
|
Hybridization protocol |
Fragmented RNA was assessed for relative length on Agilent 2100 bioanalyzer and hybridized to Affymetrix HG-U133 Plus 2.0 chips for 16 hours.
|
Scan protocol |
Affymetrix GeneChip scanner
|
Description |
EPC sampled from blood and cultured
|
Data processing |
Intensities were pre-processed with MAS5.0, and further processed with variance stablization transformation
|
|
|
Submission date |
Jul 17, 2008 |
Last update date |
Aug 28, 2018 |
Contact name |
Richard Cannon |
E-mail(s) |
[email protected]
|
Phone |
301-496-9895
|
Organization name |
NIH
|
Street address |
10 Center Drive
|
City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892-1454 |
Country |
USA |
|
|
Platform ID |
GPL570 |
Series (1) |
GSE12155 |
Characterization of a Colony Assay Used to Investigate Endothelial Progenitor Cells |
|
Relations |
Reanalyzed by |
GSE119087 |