if i understand your question correctly then, you take a human cell and combine it with insulin you then inject that/those cell(s) into the persons pancreas, and the cells divide and rapidly multiply causing the pancreas to jump back into life (it's basically a form of cloning and genetic modification) BTW I'm not a geek or a nerd or out, i just sorta' listened in that science lesson.
The insulin producing gene is "cut" out of the bacterium using enzymes. Then the gene a "put" into the bacterium using enzymes again. The bacterium is then grown and produces insulin for humans.
Biology honors grade 9 student- it uses the original genome to create acdc and to make a lot of blood cells throughout the penis
recombinant DNA formation
Sorry but we don't know his answer.. you should ask your science teaceher. and you shouldn't be getting your answers on the internet..
how would you describe genetic engineering to someone who doesn't know about biology
genetic engineering
genetic engineering
The need of pure culture of bacteria to characterize an individual species. Pure culture are also important to study the morphology and physiology of individual bacterial species, their biochemical behaviour and response to different compounds like antibiotics, which all can me alter by the influence of other species if prestent (in mixed culture) and also for isolating and studying of their molicular structure i.e. DNA or RNA. Some common ways to obtain a pure culture of bacteria are: 1 The spread plate technique. 2 The pour plate. 3 Streak plate technique.
Recombinant DNA technology can be used to genetically modify something.
Growing a new corn plant that can tolerate drought and disease. Developing rice that contains more Vitamin A. Using a bacteria to deliver chemical agents in cancer treatment. Using bacteria to mass produce human insulin.
Prokaryotic mRNA molecules are degraded by enzymes after only a few minutes . Thus bacteria can quickly alter patterns of protein synthesis in response to environmental changes.
Yes. X-rays can alter DNA, and DNA can be altered by scientists.
A plasmid is a circular double stranded DNA usually found in bacteria. Most of them do not have specific functions and altering them does not hamper the bacteria possesing them. A gene of interest can be annealed to this plasmid so as to make the concerned bacteria produce a particular product. Since the bacteria can now produce a new product, the plasmid has been used to alter the characteristics of the organism.
The advantages of using transgenic bacteria to produce human proteins are:It is very easy to alter bacterial plasmid.Moreover, bacteria can be cultured very easily and in large quantities. So, there is quick and bulk production of the required product.The proteins grow cheaply and in abundance.
site-direct mutagenesis
Altering a copyrighted painting to teach a technique is still copyright infringement as that falls under derivative works.
If you have been diagnosed recently, ask your doctor what you can do whenever you occasionally overeat. Only your doctor should tell you in what way to alter your intake of insulin, if any.
The need of pure culture of bacteria to characterize an individual species. Pure culture are also important to study the morphology and physiology of individual bacterial species, their biochemical behaviour and response to different compounds like antibiotics, which all can me alter by the influence of other species if prestent (in mixed culture) and also for isolating and studying of their molicular structure i.e. DNA or RNA. Some common ways to obtain a pure culture of bacteria are: 1 The spread plate technique. 2 The pour plate. 3 Streak plate technique.
antiseptics target the bacteria and alter the PHof their enviroment toa more basic or acidic level in which they cant live or grow in
well, we use fertilizers.
Plants
is the ability of some bacteria to alter their shape or size in response to environmental conditions
Recombinant DNA technology can be used to genetically modify something.
Clindamycin