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WSQ Domain 4: Biotechnology Part 2
Complete this form electronically.
1. Bring your notes to class.
2. Following your notes, write you 'HOT' questions to bring to class.
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WATCH! As you watch the video, take notes from the slides. Feel free to pause, rewind, rewatch as often as you like!
SUMMARY!
Please answer all questions in full sentences.
Summary Question 1
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How does bacterial transformation work? What do bacteria use it for? What do genetic engineers use it for?
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Summary Question 2
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What is cDNA? How is it made? Why is it necessary?
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Summary Question 3
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Diagram the process of genetic engineering a bacterium. 1. Begin with a plasmid and the gene of interest. 2. Show how the gene is inserted in the plasmid. 3. Show how the plasmid is incorporated into a bacterial cell. 4. Show how the cell copies the plasmid. 5. Show how the cell expresses the gene of interest. **WRITE DONE WHEN COMPLETE**
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Summary Question 4
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Explain how reporter genes (selectable markers) can be used to separate bacteria who have taken up the transformed plasmid from those who have taken up the non-transformed plasmid.
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Summary Question 5
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Explain the relationship between single nucleotide polymorphisms (“SNPs”) and restriction fragment length polymorphisms (“RFLPs”)? How are they caused and why do they matter?
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Summary Question 6
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Pick one real-world application that uses PCR and gel electrophoresis and specifically explain how each process is used in that application.
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Summary Question 7
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Compare and contrast therapeutic cloning with reproductive cloning.
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QUESTION! Be sure to write you HOT question following you notes. We will go over these in class during our WSQ discussion.
*big thanks to Crystal Kirch for originating this form and allowing me to use it!
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