Cultivation method of cross-bred wagy
A technology of bull and bovine embryos, applied in the preservation of human or animal bodies, medical science, embryonic cells, etc., to achieve the effect of improving meat quality standards and soft texture
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Embodiment 1
[0052] The acquisition and maturation culture of embodiment 1 oocyte
[0053] The oocytes obtained from the ovaries of Canadian Holstein cows collected from Canadian slaughterhouses were processed in the laboratory. The operating procedures are as follows: (a) The equipment for collecting and shipping ovaries must be cleaned in advance; (b) Prepare high-pressure sterile saline in advance, add 1% antibiotics before use, and keep warm in a water bath at 28°C until Use; (c) Collect cow ovaries with no obvious lesions and no feces contamination, and put the ovaries into a thermos bottle with pre-packed physiological saline; (d) The time from the collection of ovaries to their utilization shall not exceed 10 hours .
[0054] The procedure for extracting oocytes is as follows: (a) transfer the ovary to a wide-mouth thermos flask, pour in saline solution with 1% antibiotics at about 30°C until the ovary is submerged, and use it after cleaning the ovary; (b) 10mL syringe cover Put o...
Embodiment 2
[0061] Example 2 In vitro fertilization
[0062]The in vitro fertilization culture solution of the present invention (called 603 culture solution, its formula is shown in Table 3. The specific formula of 603 culture solution in the present embodiment is: add 50 mL of hydroxyethylpiperazine ethanesulfonic acid, heparin 0.6mL, fructose 1.2g, lactic acid 10mL, calf serum albumin 6g, phenol red 0.02g, penicillin 50IU, streptomycin 50IU, after mixing, add culture mother solution to 1000mL, adjust the pH value to 7.2) is conventional fertilization culture The improved version of TALP can change the oocyte cytoplasm to be more suitable for sperm penetration, and focus on the capacitation efficiency of sperm. Two hours before in vitro fertilization of in vitro embryos, take a four-well plate, and add 600 microliters of 603 culture medium to each well, and then put it in 39°C, 5% CO 2 incubator for pre-incubation. The frozen semen treatment in the cultivation method of the present in...
Embodiment 3
[0067] Embodiment 3 culture embryo in vitro
[0068] The configuration of the embryo culture solution of the present invention is added on the basis of the 601 culture mother solution (see Table 1 for the formula). In the present invention, the embryo culture solution is referred to as 604 culture solution for short, and the formula is shown in Table 5. In this example, the specific formula of the 604 culture solution is: 3g of glycine, 2g of alanine, 3g of arginine, 2g of glutamic acid, 2g of cystine, 5g of lysine and 5g of methionine were added to 800mL of culture mother solution , 5 g of leucine, 5 g of phenylalanine, 60 g of fetal bovine serum albumin, 0.3 g of inositol, 50 IU of penicillin, and 40 IU of streptomycin. Finally, it was sterile filtered and stored at 4°C for later use. Two hours before in vitro embryo culture, take a four-well plate and add 680 microliters of 604 culture solution to each well, then add 320 microliters of sterilized paraffin oil to the cultu...
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