Method for long-term household preservation of individual biological tissue cells and active DNA of individual biological tissue cells
A technology of tissue cells and preservation methods, applied in recombinant DNA technology, DNA preparation, special decorative structures, etc., can solve the problems of DNA pollution, reduce the storage capacity of biological information, disrupt the way of storing DNA molecules, etc., and achieve a simple production process. , good decorative effect, easy to popularize effect
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specific Embodiment approach 1
[0029] 1. Reagents needed:
[0030] 1. AA fixative: ethanol-glacial acetic acid solution, components: 95% ethanol and glacial acetic acid are prepared at 99:1;
[0031] 2. Hematoxylin staining solution, eosin staining solution, and neutral gum can all come from commercial products;
[0032] 2. Operation method
[0033] Use the oral test tube to go deep into the oral cavity, wipe the oral mucosa repeatedly, take it out, put it into a preservation bottle containing 2-5 ml of cell preservation solution (commercially available), shake, wash out the cells on the test sample into the liquid, discard the test Transfer to a centrifuge tube at 1000-2000 revolutions / centrifuge for 3-10 minutes, discard the supernatant, add 1 ml of AA fixative, suspend the precipitate and transfer it to a 1.5 ml Eppendorf tube with a disposable dropper, and let it stand for 5-20 Min, 1000-2000 revolutions / separation for 1-5 minutes, discard the supernatant, add 1 ml of distilled water, shake, 1000-2000 revo...
specific Embodiment approach 2
[0034] 1. Reagents needed:
[0035] 1. AFA fixative solution: alcohol-formalin-acetic acid solution, formaldehyde (40%), 95% ethanol and glacial acetic acid at 2:17:1;
[0036] 2. Eosin staining solution and neutral gum can all come from commercial products;
[0037] 2. Operation method
[0038] Use scissors to cut out about 30 cubic millimeters of soft tissue from the surgically removed soft tissue or from the oral mucosa of the biological individual’s remains, put it into a 1.5 ml Eppendorf tube with 1 ml AFA fixative, and let it stand for 15-30 minutes. Aspirate and discard the liquid with a pipette, add 1 ml of distilled water, shake, absorb and discard the liquid with a pipette, add a drop of eosin dye solution, let stand for 30 seconds to 2 minutes, add 1 ml of 95% ethanol, Let stand for 5-20 minutes, suck up the liquid with a pipette and discard, add 1 ml of absolute ethanol, let stand for 5-20 minutes, suck up the liquid with a pipette and discard, then add 1 ml of absolute...
specific Embodiment approach 3
[0039] This embodiment is the same as embodiment 1 or 2, except that the stained cells are put into a glass tube with an inner diameter of 1-5 mm. One end of the tube is blind, and 1-5 drops of natural neutral are added. The resin is embedded, and then the highly transparent unsaturated polyester resin is gently added until it is full and solidified, and then the highly transparent unsaturated polyester resin is wrapped and molded.
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