Preparation method of blastomere reconstructed embryo of high productive dairy cow
A blastomere, dairy cow technology, applied in the field of embryology, can solve problems such as large cell damage
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Embodiment 1
[0034] The features and advantages of the present invention can be further understood through the following detailed description in conjunction with the accompanying drawings. The examples provided are only illustrative of the method of the present invention and do not limit the rest of the present disclosure in any way. [Example 1] Preparation of in vitro mature dairy cow oocytes
[0035] (1) Put the dairy cow ovaries collected in the slaughterhouse into sterilized saline solution at 25°C with double antibodies and store them at a constant temperature for 7 hours, then bring them back to the laboratory, wash them with sterile saline at 30°C and 35°C in sequence, and wash them twice respectively. Put it in a water bath at 39°C for standby, and obtain cumulus-oocyte complexes (COCs) by aspiration with a 10 ml disposable syringe;
[0036] (2) The picked cumulus-oocyte complexes (COCs) were washed 3 times with DPBS buffer containing 5% fetal bovine serum (FBS) preheated in a 39°...
Embodiment 2
[0038] [Example 2] In vitro fertilization and culture to obtain high-quality dairy cow embryos
[0039] (1) Frozen semen of Simontal cattle is treated with BO liquid floatation method: the frozen semen of dairy cows is purchased from the Wuhan Dairy Cow Improvement Station, and the breed is Simontal dairy cows; the sperm processing method: take the frozen semen from a liquid nitrogen tank and put it into Thaw quickly in a 37°C water bath for 30-40 seconds, sterilize with 75% alcohol, cut the thin tube, put the sperm into a centrifuge tube containing 1mL BO solution, blow gently with a pipette gun, turn it upside down several times, and place in carbon dioxide Stand in the incubator for 20-30min to make the sperm float up, centrifuge the floated sperm at 1500r / min for 5min, then centrifuge twice with BO' solution at 1500r / min for 5min;
[0040] (2) Oocytes matured in vitro were digested with 2% hyaluronidase to remove cumulus cells, and then placed in in vitro fertilization flu...
Embodiment 3
[0045] [Example 3] Preparation of blastomere reconstituted embryos
[0046] (1) Digest the zona pellucida with 0.25% pronase to obtain a single blastomere from in vitro fertilized embryos developed to the 32-cell stage and above, and transfer them to TCM-199 operation drops containing 10% FBS for later use;
[0047] Use a fixed needle with an inner diameter of 40 μm and an outer diameter of 180 μm to suck oocytes from the direction of 9 o’clock on the hour hand, and make the first polar body in the direction of 1-3 o’clock. The operating system uses the pulse generated by its voltage effect to act on the cell surface through the injection needle, breaks the zona pellucida and cell membrane, and removes the genetic material including the first polar body. Piezo removes the first polar body parameters: break zona pellucida 3, break cell membrane 1; transfer the oocyte with the first polar body removed to the operation droplet with blastomeres for later use;
[0048] When the em...
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