|
Status |
Public on May 15, 2018 |
Title |
SCP2 |
Sample type |
RNA |
|
|
Source name |
Rat Schwann cell precursors
|
Organism |
Rattus norvegicus |
Characteristics |
cell type: Rat Schwann cell precursors culture conditions: Normal
|
Treatment protocol |
Rat oligodendrocyte precursors are cultured in modified Sato medium for around one week.
|
Growth protocol |
Rat Schwann cell precursors are cultured in modified Sato medium and grown.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA samples were extracted from cells using ISOGEN(NIPPON GENE) and RNeasy mini kit (QIAGEN).
|
Label |
Cy5
|
Label protocol |
Amino Allyl aRNA was synthesis by Amino Allyl MessageAmp II aRNA Amplification Kit (Ambion#1753). CyeDye Coupling and fragmentation were performed as the protocol supplied by TORAY Industries, Inc..
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|
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Hybridization protocol |
Hybridized for 16 h at 37 C with rotary shake (250 rpm). Hybridization buffer and washing protocol was followed by the protocol supplied by TORAY Industries, Inc..
|
Scan protocol |
3D-Gene Scanner ((Toray Industries Inc., Tokyo, Japan) was used for scanning. Images were quantified using Extraction(Toray Industries Inc., Tokyo, Japan).
|
Description |
Rat Schwann cells
|
Data processing |
The raw data of each spot was normalized by substitution with a mean intensity of the background signal determined by all blank spots’ signal intensities of 95% confidence intervals.
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|
|
Submission date |
May 14, 2018 |
Last update date |
May 15, 2018 |
Contact name |
Satoshi Kondo |
Organization name |
Toray Industries,Inc.
|
Street address |
10-1 tebiro 6-chome
|
City |
Kamakura |
State/province |
Kanagawa |
ZIP/Postal code |
248-8555 |
Country |
Japan |
|
|
Platform ID |
GPL22440 |
Series (1) |
GSE114441 |
Schwann cell precursor mRNA in normal culture conditions |
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