SLIDE 1
Slide 1 / 41 1 Define biotechnology. Slide 2 / 41 2 Define - - PDF document
Slide 1 / 41 1 Define biotechnology. Slide 2 / 41 2 Define - - PDF document
Slide 1 / 41 1 Define biotechnology. Slide 2 / 41 2 Define genetic engineering. Slide 3 / 41 3 Why is biotechnology as a business continually able to grow? Slide 4 / 41 4 Define cloning. Slide 5 / 41 5 What type of technology has been
SLIDE 2
SLIDE 3
7 Identify two different types of stem cells.
Slide 7 / 41
8 Identify some of the common examples of biotechnology.
Slide 8 / 41
9 What was the first animal to be cloned?
Slide 9 / 41
SLIDE 4
10 What was the first mammal to be cloned?
Slide 10 / 41
11 Describe the steps of nuclear transfer cloning.
Slide 11 / 41
12 What advantage do embryonic stem cells have
- ver adult stem cells?
Slide 12 / 41
SLIDE 5
13 Describe how embryonic stem cells have been used to date.
Slide 13 / 41
14 Describe how adult stem cells have been used to date.
Slide 14 / 41
15 What is diabetes?
Slide 15 / 41
SLIDE 6
16 Identify the technology that allowed for production of human insulin.
Slide 16 / 41
17 Briefly describe how the human insulin was produced.
Slide 17 / 41
18 How are pieces of DNA found on the genome today?
Slide 18 / 41
SLIDE 7
19 The sites where the restriction enzymes cut the DNA are known as what?
Slide 19 / 41
20 Describe what causes the DNA to move through the gel.
Slide 20 / 41
21 How was diabetes first treated? Explain why this was not successful.
Slide 21 / 41
SLIDE 8
22 List the steps of Recombinant DNA Technology.
Slide 22 / 41
23 Which macromolecule allows for genetic engineering to occur? How?
Slide 23 / 41
24 Describe how we are able to separate the gene of interest from the genome.
Slide 24 / 41
SLIDE 9
25 Which pieces of DNA would be found farthest from the starting point in a gel electrophoresis?
Slide 25 / 41
26 After we separate the gene of interest through gel electrophoresis, what is the next step in Recombinant DNA Technology?
Slide 26 / 41
27 After PCR, what happens to our gene of interest?
Slide 27 / 41
SLIDE 10
28 Identify the part of the bacteria where the gene of interest can be inserted.
Slide 28 / 41
29 Provide examples of common uses for Recombinant DNA technology.
Slide 29 / 41
30 What is the end product of PCR?
Slide 30 / 41
SLIDE 11
31 How is the gene of interest able to insert itself within the host DNA in the correct location?
Slide 31 / 41
32 What enables bacterial cells to be able to reproduce and express this gene that is newly introduced to this organism?
Slide 32 / 41
33 Identify the last step of Recombinant DNA technology.
Slide 33 / 41
SLIDE 12
34 Define gene therapy.
Slide 34 / 41
35 Differentiate between the view of genetic engineers and synthetic biologists.
Slide 35 / 41
36 How is this synthetic life different from the
- riginal bacteria cell?
Slide 36 / 41
SLIDE 13
37 Explain the importance of a DNA synthesizer.
Slide 37 / 41
38 List the steps of gene therapy.
Slide 38 / 41
39 Briefly explain the process of creating a synthetic life.
Slide 39 / 41
SLIDE 14