|
Status |
Public on Jun 16, 2020 |
Title |
control_U251_48h_rep2 |
Sample type |
RNA |
|
|
Source name |
U251, 48h
|
Organism |
Homo sapiens |
Characteristics |
cell line: U251
|
Treatment protocol |
The cells was treated with culcita novaeguineae saponin
|
Growth protocol |
Human glioma cell lines U251 was cultured in DMEM (Hyclone) supplemented with 10 % FBS (Biowest) at 37 ℃ with 5 % CO2.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 12 ug total RNA (Expression Analysis Technical Manual, 2013, Affymetrix).
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|
|
Hybridization protocol |
Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Primeview human Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
|
Scan protocol |
GeneChips were scanned using the GeneArray Scanner 3000 7G.
|
Description |
Gene expression data from U251 MG cells
|
Data processing |
The data were analyzed with rma using Affymetrix default analysis settings and global scaling as normalization method.
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|
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Submission date |
Dec 20, 2017 |
Last update date |
Jun 18, 2020 |
Contact name |
Peng-Cheng Qiu |
E-mail(s) |
qpc023@126.com
|
Phone |
86-13772051376
|
Organization name |
Fourth Military Medical University
|
Street address |
Changle West Road 169
|
City |
Xi'an |
ZIP/Postal code |
710032 |
Country |
China |
|
|
Platform ID |
GPL15207 |
Series (1) |
GSE108343 |
a New Marine-Derived Asterosaponin (CN-3) alleviated the proliferation of U251 MG cells |
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