|
Status |
Public on Aug 21, 2010 |
Title |
PaS_4factor_2 |
Sample type |
RNA |
|
|
Source name |
Bone marrow PaS (MSC), infected Oct3/4, Sox2, Klf4, and c-Myc
|
Organism |
Mus musculus |
Characteristics |
tissue: Bone marrow cell source: PaS (MSC)
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was purified with Trizol (invitrogen) and treated with Turbo DNA-free kit (Ambion) to remove genomic DNA contamination.
|
Label |
Cy3
|
Label protocol |
Total RNA from ES cells, PαS cells, OB cells, TTF cells and iPS cells were labelled with Cy3.
|
|
|
Hybridization protocol |
Samples were hybridized to a mouse Oligo Microarray (agilent) according to the manufacturer's protocol.
|
Scan protocol |
Arrays were scanned with a G2565BA Microarray Scanner System (Agilent).
|
Data processing |
Data were analysed using GeneSprings GX software (Agilent).
|
|
|
Submission date |
Aug 19, 2010 |
Last update date |
Aug 20, 2010 |
Contact name |
Yumi Matsuzaki |
E-mail(s) |
[email protected]
|
Phone |
81-3-5363-3117
|
Fax |
81-3-5363-3566
|
Organization name |
Keio University, School of Medicine
|
Department |
Physiology
|
Street address |
35 Shinanomachi
|
City |
Shinjuku |
State/province |
Tokyo |
ZIP/Postal code |
160-8582 |
Country |
Japan |
|
|
Platform ID |
GPL7202 |
Series (1) |
GSE23717 |
Purified mesenchymal stem cells are an efficient source for iPS cell induction |
|