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Freezing and resuscitation

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Freezing and resuscitation

In order to save space and reduce the occupancy rate of cages, it is possible to avoid physical or genetic pollution of mice due to factors such as external environment, microorganisms and genetic drift. Long-term stability can be achieved by freezing the genetic material in liquid nitrogen.

Freezing methods include sperm freezing and embryo freezing. The freezing and recovery comparison of the two freezing operations is as follows:

 

Freezing method

Sperm Freezing and Resuscitation

Embryo Freezing and Resuscitation

Amount of rats

≥ 2 fertile male rats aged 12-24 weeks

Three 12-24 week old fertile male rats, 15-40 less than 4 month old female rats

quantity of genetic material

15 to 20 straw sperm

Frozen 200/400 etc. Embryos

Technical features

IVF after sperm resuscitation yields large numbers of same-day-old offspring

Recipient can be transplanted directly after embryo resuscitation without IVF

Scope of application

Prefer single gene or common pure background lines (example: B6J,B6N)

Preference to monogenic/polygenic homozygous or special background lines

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