Method for improving development quality of in vitro fertilization female embryos after implantation
An in vitro fertilization and embryo technology, applied in embryo cells, biochemical equipment and methods, microorganisms, etc., can solve problems such as solutions that do not achieve expected results, reduce the development efficiency of bovine IVF embryos, and reduce the risk of sex ratio imbalance. The effect of reducing the chance of abnormal fetal development and increasing the chance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0020] Embodiment 1 mouse in vitro fertilization embryo production
[0021] 1. In vitro fertilization
[0022]ICR female mice aged 7-8 weeks were intraperitoneally injected with 5IUPMSG (Ningbo Second Hormone Factory), and 47-48h later injected with 5IUhCG (Ningbo Second Hormone Factory). Thirteen hours after the injection of hCG, the mice were sacrificed by cervical dislocation, and the oviducts were dissected and cut, placed in the preheated 37°C M2 operating solution (Sigma Company), and the enlarged part of the oviducts was cut with a syringe under a stereomicroscope to collect cumulus oocytes The complex (mature MⅡ stage oocyte) was transferred to M2 operating solution preheated at 37°C and fully washed before use. Adult healthy male rats (10-12 weeks old) were killed by decapitation, the abdominal cavity was cut open with sterilized scissors, the cauda epididymis was taken, and the sperm in the cauda epididymis was squeezed out with forceps and scissors, and put into a ...
Embodiment 2
[0032] Embodiment 2 bovine in vitro fertilization embryo production
[0033] 1. In vitro fertilization
[0034] Mature MⅡ stage oocytes obtained by hormonal superovulation were washed 3 times in fertilization fluid (BO fluid + 10 mM caffeine + 3 mg / ml BSA) and then put into well-balanced 50 μl fertilization fluid droplets (15 pieces / drop ); Sperm capacitation was carried out by the flotation method, the sperm were floated in the semen solution (BO solution + 20 μg / ml heparin sodium + 6 mg / ml BSA) for 20-30 minutes, and then 600-800 μl of the supernatant was taken and put into a 1.5ml centrifuge tube for centrifugation (1500 rpm , centrifuged for 5 min), the supernatant was discarded, and the washing was repeated once. Remove the supernatant after centrifugation, then add the semen washing solution, count the sperm, then take 50 μl of the treated semen and add it to the fertilization fluid that has been placed in the oocyte, and the final concentration of sperm is 1×10 6 Sper...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com