|
Status |
Public on Mar 12, 2020 |
Title |
QM84C21 |
Sample type |
RNA |
|
|
Source name |
0.5 M NaCl eluted Exo
|
Organism |
Mus musculus |
Characteristics |
sample type: CTL culture supernatant
|
Treatment protocol |
Murine CTL culture supernatant was subjected to DEAE column chromatograpy after concentration of deproteinization of 750 kDa MWCO ultrafiltration.
|
Growth protocol |
Murine CTL was cultured for 7days, and culture supernatant was collected.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted, and amplified with Ambion Amino Allyl aRNA kit.
|
Label |
Cy5
|
Label protocol |
Amplified aRNA was labeled with Amersham Cy5 mono-reactive dye (GE #PA25001)
|
|
|
Hybridization protocol |
Hybridization was performed with hybridyzation chamber (Takara Bio #TX711
|
Scan protocol |
3D-Gene Scanner 3000 (Toray) was used in this study.
|
Data processing |
After the image was acquired with the optimal PMT value (laser-100%), it was digitized with digitizing software.
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|
|
Submission date |
Mar 11, 2020 |
Last update date |
Mar 12, 2020 |
Contact name |
Naohiro Seo |
E-mail(s) |
seo-naohiro@clin.medic.mie-u.ac.jp
|
Organization name |
Mie University Graduate School of Medicine
|
Department |
Immuno-Gene Therpy
|
Street address |
2-174 Edobashi
|
City |
Tsu |
State/province |
Mie |
ZIP/Postal code |
514-8507 |
Country |
Japan |
|
|
Platform ID |
GPL22438 |
Series (1) |
GSE146815 |
mRNA microarray analysis of murine CTL EVs separated by ion exchange method [mRNA] |
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