Method for improving compatibility and development rate of interracial nuclear transfer embryo nucleoplasm
A technology of nuclear transfer and development rate, which is applied in the field of embryo engineering and developmental biology, and can solve the problems of low embryo development rate or normal development rate
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[0046] 6. Preparation of Human Oocyte Plastids
[0047] The undivided eggs (abandoned eggs) were collected after 24 hours of in vitro fertilization, and were transported to the somatic cell nuclear transfer operation laboratory in a 37°C warm state. After washing with PBS, a part of the eggs were taken, and the state and position of the nuclei were observed under a fluorescence microscope. Use protease to digest and remove the zona pellucida of human eggs, then place the eggs without the zona pellucida on a micromanipulator, use a microinjection needle to divide the eggs with the zona pellucida off into several ooplasmic bodies, and place them under a fluorescent microscope Observe, pick out the cytoplast containing the nucleus (chromosome), and the remaining cytoplast without nucleus can be used for cytoplasm supplementation.
[0048] 7. Preparation of nuclear transfer embryos composed of three parts: human oocyte plastid-human cell-goat enucleated egg
[0049] Place th...
Embodiment 1
[0059] Effects of Human Egg Cytoplasm Supplementation on the Development of Human Nucleus-Enucleated Goat Egg Reconstructed Embryo
[0060] 1 Materials and methods:
[0061] 1.1.2 Reagents
[0062] All embryo-grade reagents are Sigma products unless otherwise stated.
[0063] 1.2 Method
[0064] 1.2.1 Collection of donor oocytes
[0065] Dairy goats were routinely superovulated with FSH, and 29-30 hours after LRH injection, the oocytes were recovered by surgery, and the oviducts were washed with F-10 (Gibco) culture medium containing 5% calf serum (FCS, Gibco) . Oocytes are collected and hyaluronidase removes attached granulosa cells. The collected oocytes were cultured in M16 solution, 37.5°C, 5% carbon dioxide incubator.
[0066] 1.2.2 Donor cells
[0067] Cut human foreskin tissue or aborted fetal skin into 1cm 2 Tissue blocks, or digested into single cells with trypsin, cultured in DMEM medium (plus 10-20% fetal calf serum, FCS), passaged, and genetical...
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