Method of extracting anti-intestinal cancer active protein from nostoc commune
A technology of active protein and cabbage, which is applied to the preparation methods of peptides, chemical instruments and methods, anti-tumor drugs, etc., can solve problems such as reports on anti-tumor active proteins of cabbage, which have not been seen, and achieve the effect of low cost.
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Embodiment 1
[0021] The preparation method of the anti-intestinal cancer active protein of Chinese cabbage, the steps are as follows:
[0022] (1) Dried the natural ground vegetables and crushed them into powder with a grinder.
[0023] (2) Take 25g of ground vegetable powder, add 400ml of PBS buffer, stir on a stirrer, soak overnight at 4°C for 12 hours, centrifuge at 11000rpm for 25min, take the supernatant, add 150ml of PBS buffer to the filter residue, and do the same as above , the two extracts are combined to obtain the crude extract of Dipodella protein.
[0024] (3) Slowly add 2 times the volume of acetone pre-cooled at -20°C to the crude extract of the Chinese cabbage protein obtained in (2), stir slowly, then place it at -20°C for 1 hour, and centrifuge at 11,000 rpm for 30 minutes , discard the supernatant, collect the precipitate, place the precipitate at -20°C for 30 minutes, completely volatilize the acetone, and freeze-dry the precipitate to obtain 48 mg of crude protein of...
Embodiment 2
[0028] DLD1, SW620, HL-7702 cells in the logarithmic growth phase were treated with 1×10 4 per well into a 96-well culture plate. 37°C with 5% CO 2 After incubating in the incubator for 24 hours, the active protein of Dipis praecox was added at concentrations of 0.08, 0.16, 0.24, and 0.32 mg / ml respectively, and five replicate wells were set up, and PBS buffer was used as a control. After incubation for 48 hours, discard the medium in the wells, wash twice with PBS, add new medium, add 20 l of MTT solution (5 mg / ml) to each well, continue incubation for 4 hours, and terminate the culture. Carefully aspirate and discard the culture supernatant in the wells, add 150l DMSO to each well, and shake on a shaker for 10min to fully dissolve the crystals. At a wavelength of 570 nm, the light absorbance of each well was measured on an enzyme-linked immunosorbent monitor.
[0029] The active protein of Dipis pratense obtained in the present invention is used for the above-mentioned in...
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