This document discusses the use of animals in biotechnology and medical research. It explains that animals are useful models for human physiology and that many medical advances like vaccines and surgical techniques were developed using animals. It then discusses why single cells are not sufficient and why specific animals like zebrafish, rats, mice, dogs, monkeys and chimpanzees are used. The document also covers cloning techniques in animals and some limitations of cloning. Finally, it provides an example of how spider silk genes were transferred to goats to produce silk proteins for potential use in bulletproof vests.
This document discusses the use of animals in biotechnology and medical research. It explains that animals are useful models for human physiology and that many medical advances like vaccines and surgical techniques were developed using animals. It then discusses why single cells are not sufficient and why specific animals like zebrafish, rats, mice, dogs, monkeys and chimpanzees are used. The document also covers cloning techniques in animals and some limitations of cloning. Finally, it provides an example of how spider silk genes were transferred to goats to produce silk proteins for potential use in bulletproof vests.
This document discusses the use of animals in biotechnology and medical research. It explains that animals are useful models for human physiology and that many medical advances like vaccines and surgical techniques were developed using animals. It then discusses why single cells are not sufficient and why specific animals like zebrafish, rats, mice, dogs, monkeys and chimpanzees are used. The document also covers cloning techniques in animals and some limitations of cloning. Finally, it provides an example of how spider silk genes were transferred to goats to produce silk proteins for potential use in bulletproof vests.
between animal and man exist. ■Polio vaccine was developed using animals. ■Cataract surgery techniques were perfected on animals. ■Dialysis for the end-stage kidney disease was first tested in animals. Why can’t we just test it in a group of cell in a petri dish?
■It is not enough because new drugs
and medical procedures have effects beyond single cells in tissues and organs and must be tested in animals to determine the impact of the treatment on an entire organism. Why zebra fish? ■ Brachydanio rerio ■ Fast reproduction ■ Average progeny of female eggs can exceed 200 ■ Zebra eggs complete embryogenesis in about 120 hours ■ Toxicity test can be observed in 5 days. ■ If toxic to zebra fish, then it is toxic to humans. Why rats/mice?
■ Rats are more commonly used because of their
size and physiology and more human responses to drugs ■ Rats are superior to mice for many early drug toxicity tests because of their physiology and more human- like responses to drugs. ■ Large size of rats facilitates surgical and physiologic experimentation. Why Dogs?
■If fish, rats and mice are not
the best to use. ■Lungs and cardiovascular system of dogs and humans are similar making them a better choice for the study of heart disease and lung disorders. Monkeys and Chimpanzees ■Conduct of HIV/ AIDS research on them because they are the only known animal that share humans’ vulnerability to the virus Cloning
■Animal that is grown from one cell of
its parent and that has exactly the same genes as its parent 1st step- collect eggs
Animal Cloning from the animal of
interest and the culture for cloning
10 11 Enucleation
■A process of removing the DNA in
the nucleus of a cell. Limitations of cloning
■The donor cell must come to a LIVING
organism ■Attitudes and behaviors are shaped by experiences ■Success rate is low ■Clones may become older before their time Bulletproof vests ■Bio-steel is made from spider web proteins, which is one of the strongest fibers on earth. ■The gene that governs the production of spider silk proteins has been successfully transferred into goats, and those goats reproduced, passing the new gene to their offspring. ■“silk-milk” ■Silk protein is purified in the goats milk and