|
Status |
Public on Aug 27, 2015 |
Title |
IL-22-2 [miRNA] |
Sample type |
RNA |
|
|
Source name |
IL-22-2 [miRNA]
|
Organism |
Homo sapiens |
Characteristics |
cell line: HaCaT agent: IL-22 stimulation
|
Treatment protocol |
To prepare them for recombinant human IL-22 (Sangon Biological Engineering Technology Company, Shanghai, China) treatment, HaCaT cells were starved in serum-free DMEM for 24 h and then treated with IL-22 (100 ng/ml) in serum-free DMEM for another 24 h or not treated.
|
Growth protocol |
HaCaT cells were cultured in DMEM supplemented with 10% fetal bovine serum (FBS),100 U/ml penicillin and 100µg/ml streptomycin at 37℃ in a humidified atmosphere containing 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 15ug total RNA
|
|
|
Hybridization protocol |
Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 48C on GeneChip Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
|
Scan protocol |
GeneChips were scanned using the GeneChip2 Scanner 3000 7G
|
Data processing |
GeneChip Command Console Software (AGCC).
|
|
|
Submission date |
Aug 26, 2015 |
Last update date |
Aug 27, 2015 |
Contact name |
Meng Jiang |
E-mail(s) |
1037447134@qq.com
|
Phone |
15066142801
|
Organization name |
Qilu hospital
|
Street address |
lixia street
|
City |
Jinan |
State/province |
Shandong |
ZIP/Postal code |
250012 |
Country |
China |
|
|
Platform ID |
GPL19117 |
Series (1) |
GSE72396 |
Expression data from HaCaT cells stimulated by IL-22 |
|