A mouse embryo transplantation preservation tool and its manufacturing method
A technology of mouse embryos and manufacturing methods, applied in the preservation of human or animal bodies, medical science, animal delivery, etc., to achieve the effects of avoiding the decline in embryonic development rate, rapid operation, and reducing time
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Embodiment 1
[0035]This embodiment is the mouse embryo transplantation and preservation tool described in the present invention, comprising Pasteur tube 1, centrifuge tube 2, syringe 3 and rubber piston 4, the specific structure and connection relationship are: the rubber piston 4 is inserted from the tail The jacket of the syringe 3, cut off a part of the volume of the cone of the syringe jacket appropriately, so that the width of the cone mouth is equal to the width of the outer diameter of the Pasteur tube 1, properly cut off the two wings of the jacket of the syringe 3, so that the length of the two wings is equal to or slightly greater than the diameter of the centrifuge tube 2, Insert the jacket of the syringe 3 into the centrifuge tube 2, fix the jacket so that the jacket cannot move up and down in the centrifuge tube 2, and the Pasteur tube 1 is fixed on the cone of the jacket.
[0036] The centrifuge tube 2 is a commonly used 15mL plastic centrifuge tube with a diameter of 1.75cm, ...
Embodiment 2
[0041] like Figure 1 to Figure 6 As shown, the present embodiment is a manufacturing method of the mouse embryo transplantation preservation device according to the present invention, comprising the following steps:
[0042] (1) Take a new sterile 15mL centrifuge tube 2 without pyrogen, add 10.5mL autoclaved water to the centrifuge tube and perform autoclaving;
[0043] (2) Take a new sterile 1mL syringe 3 without pyrogen, discard the needle, take out the core rod, remove the rubber piston, and then insert the rubber piston 4 into the jacket from the tail;
[0044] (3) Use scissors to cut off a part of the cone head of the jacket to widen the mouth of the cone head with a width of 0.6-0.8 cm. After cutting, use Pasteur tube 1 to try to fix it so that the graft tube can not be fixed up and down. The left and right movement shall prevail, and the cone head of such a width can fix the Pasteur tube;
[0045] (4) Properly cut off the two wings of the jacket of the syringe 3 so t...
Embodiment 3
[0051] This example is an example of the in vitro preservation effect of using the mouse embryo transplantation preservation tool of the present invention.
[0052] 1. Add 0.2mL of normal saline, PBS or transplantation liquid to the syringe jacket, and add transplantation fluid to the jacket;
[0053] 2. The three-stage method of the Pasteur tube absorbs 15-20 fertilized eggs, inserts the Pasteur tube with the embryos into the cone mouth of the jacket, and keeps it vertical until it is inserted into the jacket under the liquid surface, about 0.5 below the liquid surface. about mm. Finally, put the whole device into a water bath at 39°C to heat it in a water bath, store it in vitro for about 20 minutes, then take out the Pasteur tube with fertilized eggs, blow all the embryos out and transfer them to a culture dish for continuous culture. The implementation method of the comparative example in the present invention is that the Pasteur tube three-stage method draws 15-20 fertil...
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