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Status |
Public on May 01, 2024 |
Title |
LN229_DMSO CTRL_48hr_rep2 |
Sample type |
RNA |
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Source name |
LN229
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Organism |
Homo sapiens |
Characteristics |
treatment: Vehicle control
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Treatment protocol |
Cells were seeded in 6-well plates and then incubated overnight to allow cells to attach. Cells were harvested after the treatment of 10 microM Momordicine or DMSO control for 48 hrs.
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Growth protocol |
Both cells were grown in DMEM medium with 2% FBS.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using Trizol according to manufacturer's protocol.
|
Label |
Cy5
|
Label protocol |
The 1 microg of total RNA was reverse-transcribed and amplified using MessageAmpTM aRNA Amplification Kit (Ambion). Indirect labeling the aa-UTP whereon by NHS-CyDye (Cy5, Amershan).
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Hybridization protocol |
HOA v7.1 arrays were pre-heat at 60℃ for 10 mins, rehydrated by 100% ethanol following with deionized water. The slides were pre-hybridized with 5x SSPE, 0.1% SDS and 1% BSA at 42℃ for 2 hour. After the pre-hybridization, 5 microg Cy5-labeled aRNA was hybridize on HOA in the presentation of the Phalanx OneArray hybridization buffer in duplication.
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Scan protocol |
The arrays were scanned by Agilent G2505C scanner (635nm) and quantify the fluoresence intensity.
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Data processing |
Data processing was performed and calculated by limma package (Bioconductor). The control probes were filtered out and then normalized by the median scaling method between technical replicates. Pair-wise comparisons between samples were calculated by empirical bayes statistics and presented by log2 ratio and p-value.
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Submission date |
May 03, 2023 |
Last update date |
May 01, 2024 |
Contact name |
Yung Lung Chang |
E-mail(s) |
ylchang@mail.ndmctsgh.edu.tw
|
Organization name |
National Defense Medical Center
|
Department |
Biochemistry
|
Street address |
Rm. 7309, 7F., No.161, Sec. 6, Minquan E. Rd., Neihu Dist.
|
City |
Taipei |
ZIP/Postal code |
114 |
Country |
Taiwan |
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Platform ID |
GPL21282 |
Series (1) |
GSE231550 |
Momordicine I Suppresses Glioma Growth by Promoting Apoptosis and Impairing Mitochondrial Oxidative Phosphorylation |
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