Long non-coding RNA related to melanoma and application thereof
A melanoma, non-coding technology, applied in the direction of DNA / RNA fragments, recombinant DNA technology, microbial measurement / inspection, etc., to achieve the effect of improving the survival rate
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Embodiment 1
[0024] Detection of the expression of LncRNA-FA2H-2 in melanoma cancer tissues and adjacent tissues
[0025] 1. Research object
[0026] 20 cases of melanoma cancer tissues and corresponding paracancerous tissues were selected for the experiment.
[0027] 2. Tissue RNA Extraction
[0028] (1) Put about 50 mg of tissue into a mortar, add a small amount of liquid nitrogen, and grind quickly. After the tissue becomes soft, add a small amount of liquid nitrogen for grinding again, and repeat three times;
[0029] (2) Add 1ml Trizol, use an electric homogenizer to homogenize for 2 minutes, transfer to a centrifuge tube after homogenization, and place at room temperature for 5 minutes;
[0030] (3) Centrifuge at 12000rpm for 5 minutes, take the supernatant, and remove the precipitate;
[0031] (4) Add 200ul of chloroform, shake and mix, and let stand at room temperature for 15 minutes;
[0032] (5) Centrifuge at 12000rpm at 4°C for 15min;
[0033] (6) Take the supernatant (be c...
Embodiment 2
[0069] Knockdown of LncRNA-FA2H-2 Gene
[0070] 1. siRNA design
[0071] si-RNA-1
[0072] 5'-AUUCUUCUGACAUGUUUCCUG-3'
[0073] 5'-GGAAACAUGUCAGAAGAAUGC-3'
[0074] si-RNA-2
[0075] 5'-UCACAUUCAAUAUGUACAGCU-3'
[0076] 5'-CUGUACAUAUUGAAUGUGAAU-3'
[0077] si-NC
[0078] 5'-ACAGAGCCUCGCCUUUGCCGAU-3'
[0079] 5'-CUUGCACAUGCCGGAGCCGUU-3'
[0080] 2. Cell Culture
[0081] Human melanoma cell line A357 was cultured in high-glucose DMEM medium (10% fetal bovine serum) at 37°C, 5% CO 2 .
[0082] 3. siRNA transfection
[0083] (1) The day before transfection, 2×10 5 A357 cells were seeded onto 6-well culture plates at 37 °C, 5% CO 2 After culturing in the incubator for 24 hours, transfect according to the instructions of Lipofectamine 2000;
[0084] (2) The experimental groups were divided into si-NC group, si-RNA-1 and si-RNA-2.
[0085] 4. Real-time quantitative PCR detection of LncRNA-FA2H-2 gene expression after knockdown
[0086] (1) Extraction of total cellular...
Embodiment 3
[0094] 1. Cell Proliferation Experiment
[0095] (1) Inoculate A357 in a 96-well plate at a cell density of 5000 cells / ml, 200 μl per well, set up 3 replicate wells for each group, place at 37°C, 5% CO 2 Static culture in the incubator;
[0096] (2) A357 cells were transfected with si-NC, si-RNA-1, and si-RNA-2 respectively. 4 hours before the end of the culture, 20 μl of 5 mg / ml MTT solution was added to each well, and the culture was continued at 37°C and 5% CO2 Stand in the box and cultivate until the end;
[0097] (3) Aspirate and discard the culture medium in the wells, add 150 μl DMSO to each well, shake horizontally for 10 min, detect the absorbance at 492 nm with a microplate reader, and draw the growth curve.
[0098] (4) SPSS19.0 statistical software was used to establish a database and conduct statistical analysis. The measurement data were expressed as mean ± standard deviation. The comparison of the means of the two groups was carried out by independent sample t...
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