New application of ethyl gallate to osteosarcoma treatment
A technology of ethyl gallate and osteosarcoma, which is applied in the field of pharmaceutical application of ethyl gallate, and can solve problems such as unreported research
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Embodiment 1
[0026] Example 1: During the culturing process of the revived U2-OS osteosarcoma cell line, the cell medium was changed as needed, and after the cell adherent growth area reached 80% of the bottom of the cell bottle, the culture medium was poured out, and the culture medium was added to The sampler draws 2mL PBS into the culture bottle, closes the lid, shakes it several times, pours off the PBS, and repeats this operation once. Use a pipette to draw 1 mL of trypsin into the culture bottle, screw the cap tightly, and place the culture bottle flat so that the trypsin can infiltrate the culture surface. Observed under an inverted microscope, if the cells become a single round shape, it is necessary to terminate the trypsin digestion. After wiping with alcohol cotton, put it into the ultra-clean workbench, pipette 1mL of fresh medium into the culture bottle, use a pipette gun to suck the liquid in the culture bottle and blow the cell culture surface of the culture bottle, and the ...
Embodiment 2
[0027] Example 2: For the passaged cells, pour out the culture medium, suck 2mL PBS into the culture bottle with a sampler, close the lid, shake it several times, pour out the PBS, and repeat this operation once. Use a pipette to draw 1 mL of trypsin into the culture bottle, screw the cap tightly, and place the culture bottle flat so that the trypsin can infiltrate the culture surface. Observed under an inverted microscope, if the cells become a single round shape, it is necessary to terminate the trypsin digestion. After wiping with alcohol cotton, put it into the ultra-clean workbench, pipette 1mL of fresh medium into the culture bottle, use a pipette gun to suck the liquid in the culture bottle and blow the cell culture surface of the culture bottle, and the liquid becomes turbid. Dilute the above-mentioned digested cells with fresh medium, and blow to disperse, absorb a little cell suspension, and drop it on the edge of the cover slip, so that the suspension fills the spac...
Embodiment 3
[0028] Example 3: For the subcultured cells, discard the culture medium, suck 2mL PBS into the culture bottle with a sampler, close the lid, shake it several times, pour out the PBS, and repeat this operation once. Use a pipette to draw 1 mL of trypsin into the culture bottle, screw the cap tightly, and place the culture bottle flat so that the trypsin can infiltrate the culture surface. Observed under an inverted microscope, if the cells become a single round shape, it is necessary to terminate the trypsin digestion. After wiping with alcohol cotton, put it into the ultra-clean workbench, pipette 1mL of fresh medium into the culture bottle, use a pipette gun to suck the liquid in the culture bottle and blow the cell culture surface of the culture bottle, and the liquid becomes turbid. Dilute the above-mentioned digested cells with fresh medium, and blow to disperse, absorb a little cell suspension, and drop it on the edge of the cover slip, so that the suspension fills the sp...
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