Difference between revisions of "Intracytoplasmic Sperm Injection - Anatomy & Physiology"

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|backcolour =EED2EE
 
|linkpage =Reproductive System - Anatomy & Physiology
 
|linktext =Reproductive System
 
|maplink = Reproductive System (Content Map) - Anatomy & Physiology
 
|sublink1=Reproductive System - Anatomy & Physiology#Reproductive Technologies
 
|subtext1=REPRODUCTIVE TECHNOLOGIES
 
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* Common in human, effective for laboratory mice.
 
* Common in human, effective for laboratory mice.
* Sperm need not be [[Copulation_-Sperm_in_the_Female_Tract_-_Anatomy_%26_Physiology#Capacitation|capacitated]], they can be epididymal,testicular or even a spermatid.
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* Sperm need not be [[Sperm in the Female Tract - Anatomy & Physiology#Capacitation|capacitated]], they can be epididymal,testicular or even a spermatid.
 
** Only requirement is genes and cytoplasm
 
** Only requirement is genes and cytoplasm
 
** Even dead freeze-dried sperm have been effective in mice.
 
** Even dead freeze-dried sperm have been effective in mice.
 
* Abnormalities are frequent.
 
* Abnormalities are frequent.
* Power is in the hands of the operator, as it bypasses the process of [[Copulation_-Sperm_in_the_Female_Tract_-_Anatomy_%26_Physiology|selection in the female tract]].
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* Power is in the hands of the operator, as it bypasses the process of [[Sperm in the Female Tract - Anatomy & Physiology|selection in the female tract]].
** Operator must select a single sperm to inject directly into the [[The_Ovary_-_Oocytes_-_Anatomy_%26_Physiology|Oocyte]] under a microscope.
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** Operator must select a single sperm to inject directly into the [[Oogenesis - Anatomy & Physiology|Oocyte]] under a microscope.
* [[The_Ovary_-_Oocytes_-_Anatomy_%26_Physiology|Oocyte]] then placed in cell culture for development.
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* [[Oogenesis - Anatomy & Physiology|Oocyte]] then placed in cell culture for development.
  
  
[[Category:Reproductive System]]
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[[Category:Reproductive Technologies]]
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[[Category:Bullet Points]]

Latest revision as of 13:49, 5 July 2012

  • Common in human, effective for laboratory mice.
  • Sperm need not be capacitated, they can be epididymal,testicular or even a spermatid.
    • Only requirement is genes and cytoplasm
    • Even dead freeze-dried sperm have been effective in mice.
  • Abnormalities are frequent.
  • Power is in the hands of the operator, as it bypasses the process of selection in the female tract.
    • Operator must select a single sperm to inject directly into the Oocyte under a microscope.
  • Oocyte then placed in cell culture for development.