Cell processing kit and using method therefor
A kit and cell technology, applied in the direction of biomass post-treatment, biomass pre-treatment, test sample preparation, etc., can solve the problems of cell deformation, affecting cell observation, and high price, so as to reduce psychological pressure and make films Time flexibility and the effect of improving the diagnosis rate
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Embodiment 1
[0051] 1. Composition of specimen preservation solution:
[0052] Contains: Hexanol: 40%, Isopropanol: 40%, Sodium Chloride: 9.8%, Tris Buffer: 10%;
[0053] 2. Separation cleaning solution: 20% polysucrose and 9.8% sodium chloride solution;
[0054] 3. Coating dilution base solution: the main component is 0.01% poly-lysine aqueous solution;
[0055] 4. Cell stock solution: the main component is 70% ethanol.
Embodiment 2
[0057] The method for using the cell treatment kit comprises the following steps:
[0058] A: Immediately put the collected specimens into the specimen preservation solution. If a specimen collection brush with a detachable head is used, put the brush head of the specimen brush into the specimen preservation solution, tighten the bottle cap, and transfer to the film production laboratory.
[0059] B: Add 4 ml of separation washing solution to the centrifuge tube.
[0060] C: After the specimen stays in the preservation solution for 30 minutes, place the specimen preservation solution bottle in a vortex mixer for 3 minutes, fully suspend, and gently pour it into a centrifuge tube with an inclined tube wall, so that the specimen preservation solution is separated from the cleaning solution. on the liquid surface.
[0061] D: Place the centrifuge tube in a centrifuge for 10 minutes, and the speed of the floating bucket centrifuge is 900g.
[0062] E: Take out the centrifuge tub...
Embodiment 3
[0067] The method for using the cell treatment kit comprises the following steps:
[0068] A: Put the brush head of the collected specimen brush into the specimen preservation solution, tighten the bottle cap, and transfer it to the film production laboratory.
[0069] B: Add 4 ml of separation washing solution to the centrifuge tube.
[0070] C: After the specimen stays in the preservation solution for 30 minutes, place the specimen preservation solution bottle in a vortex mixer for 3 minutes, fully suspend, and gently pour it into a centrifuge tube with an inclined tube wall, so that the specimen preservation solution is separated from the cleaning solution. on the liquid surface.
[0071] D: Place the centrifuge tube in a centrifuge for 10 minutes, and the barrel centrifuge rotates at 1100g.
[0072] E: Take out the centrifuge tube from the centrifuge, pour off the supernatant immediately, and place it upside down on an absorbent paper towel to dry up the remaining liquid...
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