Unlock instant, AI-driven research and patent intelligence for your innovation.

Culture method for increasing in-vitro survival rate of mammal embryos

A technology of mammals and culture methods, which is applied in the field of culturing to improve the survival rate of mammalian embryos in vitro, and can solve the problems that embryos are prone to damage or death, low embryo survival rate, and difficult to ensure stable temperature and atmosphere of the incubator, etc. To achieve the effect of simple structure, guaranteed survival rate and quick adjustment

Active Publication Date: 2019-12-31
ZHEJIANG UNIV
View PDF4 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In the existing culture method, after the embryos are placed in the incubator, the operator needs to observe or operate the embryos frequently. At this time, the door of the incubator needs to be opened, and during the operation, the environment in the box will change. The gas exchange with the outside air makes the environment in the box affected and changes, it is difficult to ensure that the incubator is always maintained in a stable temperature and atmosphere environment, the embryos are prone to damage or death, and the embryo survival rate is low

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Culture method for increasing in-vitro survival rate of mammal embryos
  • Culture method for increasing in-vitro survival rate of mammal embryos
  • Culture method for increasing in-vitro survival rate of mammal embryos

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] A culture method for improving the survival rate of mammalian embryos in vitro, including the following steps:

[0033] (1) Obtain sheep oocytes from the ewe and place them in a mature culture medium, culture in an incubator for 20 hours to obtain mature sheep oocytes; among them, the mature culture medium is an existing technology and can be selected according to actual needs , Do not repeat;

[0034] (2) Put mature sheep oocytes and sperm into the fertilization culture medium, and culture them in an incubator for 18 hours for fertilization to obtain early sheep embryos; the temperature in the incubator is maintained at 38°C and the gas concentration is maintained at 5% CO2; among them, the fertilization culture medium is TCM199 culture medium containing 3% goat serum;

[0035] (3) Wash the fertilized sheep embryos with TCM199 culture medium repeatedly, then put them in the sheep embryo in vitro culture medium, and place them in an incubator for embryo in vitro culture. The ...

Embodiment 2

[0046] A culture method for improving the survival rate of mammalian embryos in vitro, including the following steps:

[0047] (1) Obtain sheep oocytes from ewes and place them in mature culture medium, culture in an incubator for 24 hours to obtain mature sheep oocytes; among them, mature culture medium is the existing technology, which can be selected according to actual needs , Do not repeat;

[0048] (2) Put mature sheep oocytes and sperm into the fertilization culture medium, and culture them in an incubator for 24 hours for fertilization to obtain early sheep embryos; the temperature in the incubator is maintained at 39°C and the gas concentration is maintained at 5% CO2; among them, the fertilization culture medium is TCM199 culture medium containing 3% goat serum;

[0049] (3) Wash the fertilized sheep embryos with TCM199 culture medium repeatedly, then put them in the sheep embryo in vitro culture medium, and place them in an incubator for embryo in vitro culture. The tempe...

Embodiment 3

[0051] A culture method for improving the survival rate of mammalian embryos in vitro, including the following steps:

[0052] (1) Obtain sheep oocytes from ewes and place them in mature culture medium, culture in an incubator for 22 hours to obtain mature sheep oocytes; among them, mature culture medium is the existing technology, which can be selected according to actual needs , Do not repeat;

[0053] (2) Put mature sheep oocytes and sperm into the fertilization culture solution together, and culture them in an incubator for 20 hours for fertilization to obtain early sheep embryos; the temperature in the incubator is maintained at 38°C and the gas concentration is maintained at 5% CO2; among them, the fertilization culture medium is TCM199 culture medium containing 3% goat serum;

[0054] (3) Wash the fertilized sheep embryos with TCM199 culture medium repeatedly, then put them in the sheep embryo in vitro culture medium, and place them in an incubator for embryo culture in vitro...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a culture method for increasing the in vitro survival rate of mammal embryos. The method comprises the following steps: (1) taking sheep oocytes from ewes, putting the sheep oocytes into a maturation culture solution, and performing culturing in an incubator for 20-24 hours to obtain maturated sheep oocytes; (2) putting the mature sheep oocytes and sperms into a fertilization culture solution together, performing culturing in an incubator for 18-24 hours, and performing fertilizing to obtain early sheep embryos; and (3) repeatedly washing the fertilized sheep embryos with a TCM199 culture solution, then putting the sheep embryos into a sheep embryo in-vitro culture solution, putting the sheep embryos into an incubator for embryo in-vitro culture, and maintaining thetemperature in the incubator at 38-39 DEG C and the gas concentration at 5% CO2. The incubator comprises a culture chamber, a chamber door and a gas concentration adjusting chamber communicated withthe culture chamber; and a plurality of culture bins are arranged in the culture chamber, and the plurality of culture bins are respectively provided with a culture medium placing rack and a partitiondevice. The environment in the incubator is stable, so that the survival rate of the embryos is guaranteed.

Description

Technical field [0001] The invention belongs to the technical field of in vitro culture of sheep embryos, and particularly relates to a culture method for improving the in vitro survival rate of mammalian embryos. Background technique [0002] In vitro fetal culture refers to placing embryos in an incubator. The incubator maintains a constant temperature and a constant concentration of carbon dioxide to simulate the physiological environment of the uterus. The embryos in the culture medium interact with and exchange substances with them to achieve embryo growth. In the existing culture method, after the embryo is placed in the incubator, the operator needs to frequently observe or operate the embryo. At this time, the door of the incubator needs to be opened, and the environment inside the incubator will be changed during the operation. The gas exchange with the outside air causes the environment inside the box to be affected and change. It is difficult to ensure that the incubat...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12N5/073C12N5/075C12M3/00C12M1/34C12M1/04
CPCC12N5/0604C12M23/34C12M41/34C12M21/08C12M27/20C12M29/26C12M41/24
Inventor 邱寒峰吴婷徐雅萍董信阳
Owner ZHEJIANG UNIV