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Status |
Public on Jun 21, 2017 |
Title |
BEAS-2B CTRL, treated with doxycycline for 48h |
Sample type |
RNA |
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|
Source name |
BEAS-2B cell line stably transduced with a CTRL vector, treated with doxycycline for 24h
|
Organism |
Homo sapiens |
Characteristics |
cell line: BEAS-2B protocol: control treatment: doxycycline
|
Treatment protocol |
BEAS-2B CTRL and TTF-1 cell lines were treated with 1 ug/ml Doxycycline for 48 h before RNA was harvested
|
Growth protocol |
BEAS-2B cells were cultured with 1% (v/v) FCS-containing Ham F-12 supplemented with bovine insulin (5 ug/mL), human transferrin (5 ug/mL), 100 nM hydrocortisone, 200 pM triiode thyronine, penicillin (100 IU/mL), and streptomycin (100 ug/mL) at 37°C with 5% CO2
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using the miRNeasy kit (Qiagen, Valencia, CA)
|
Label |
FAM
|
Label protocol |
Total RNA was converted into cDNA using the megaplex reverse transcriptase reaction. The megaplex reaction contained a specific stem-loop primer for each of the mature target microRNA's. The cDNA was subjected to a pre-amplification PCR. The diluted pre-amplification products served as substrates for TaqMan quantitative PCR reactions.
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Hybridization protocol |
n/a
|
Scan protocol |
n/a
|
Description |
Control BEAS-2B CTRL 48h miRNA
|
Data processing |
Normalization was carried out with the expression level of RNU44.
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|
|
Submission date |
Jun 29, 2016 |
Last update date |
Jun 21, 2017 |
Contact name |
Takashi Takahashi |
Organization name |
Aichi Cancer Center
|
Street address |
1-1 Kanokoden, Chikusa-ku
|
City |
Nagoya |
State/province |
Aichi |
ZIP/Postal code |
464-8681 |
Country |
Japan |
|
|
Platform ID |
GPL11316 |
Series (2) |
GSE83838 |
TTF-1-regulated miR-532-5p targets KRAS and MKL2 oncogenes and induces apoptosis in lung adenocarcinoma [rt-pcr] |
GSE83839 |
TTF-1-regulated miR-532-5p targets KRAS and MKL2 oncogenes and induces apoptosis in lung adenocarcinoma |
|