Application of ginsenoside Rg5 in resisting melanoma
A ginsenoside and anti-melanin technology, applied in the field of biomedicine, can solve the problems that the influence of melanoma cell growth is not clear or not
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Embodiment 1
[0027] Antiproliferative effect of ginsenoside Rg5 on mouse skin melanoma cells B16F10.
[0028] The effect of Rg5 on the proliferation of mouse skin melanoma cells B16F10 was evaluated by MTT assay and morphological observation. Mouse skin melanoma cells B16F10 in the logarithmic growth phase were seeded in a 96-well plate at a density of 5x103 cells / well, with 100 μl of medium per well. After 24 hours, the cells were completely attached to the wall, and the treatment groups were given different concentrations of Rg5 for 24 hours and 48 hours, respectively. The administration concentrations of Rg5 were 1, 3, 10, 30, 100, 300 μmol / L, respectively. After the drug intervention was completed, the morphology of living cells was observed under a microscope. Discard the old medium, wash the cells with PBS, add 10 μl of MTT reagent (5.0 mg / ml) to each well, and incubate at 37°C for 4 hours in the dark. After incubation, add 100 μl DMSO to each well and shake well. Using a micropl...
Embodiment 2
[0032] Inhibitory migration of mouse skin melanoma cells B16F10 by Rg5.
[0033] The cell scratch test was used to evaluate the inhibitory effect of Rg5 on cell migration of mouse skin melanoma cells B16F10 treated for 12h and 24h. Take a 6-well plate, draw 5 parallel lines with a marker pen at the bottom of the 6-well plate, take mouse skin melanoma cells B16F10 in the logarithmic growth phase, and inoculate them in a 6-well plate at an appropriate density. After 24 hours, the cell fusion rate When it reaches 100%, use a 200 μl pipette tip to scratch the cells perpendicular to the parallel line at the bottom of the 6-well plate, wash the cells three times with PBS, and wash away the scratched dead cells. Serum-free medium was added to the control group, serum-free medium containing different concentrations of Rg5 was added to the treatment group, and the scratch widths of each group were photographed under an inverted microscope at 0h, 12h, and 24h, and five corresponding scr...
Embodiment 3
[0036] Pro-apoptotic effect of ginsenoside Rg5 on mouse skin melanoma cells B16F10.
[0037] DAPI staining and flow cytometry were used to evaluate the effects of different concentrations on the apoptosis of mouse skin melanoma cells B16F10 after 24 hours of exposure. Mouse skin melanoma cells B16F10 in the logarithmic growth phase were inoculated in 6-well plates and used Different concentrations of ginsenoside Rg5 were processed. After 24 hours of drug action, wash with PBS three times and fix with 4% paraformaldehyde for 1 hour. Use DAPI reagent to seal the slides at room temperature, and after drying, observe the cells under a microscope and collect image data.
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