Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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Above are the results of gel electrophoresis following digestion with restriction enzymes. What is the total length of the DNA fragment?
Which enzyme, HindIII or EcoRI, produced a larger fragment?
What part of DNA causes it to be negatively charged in order for electrophoresis to work?
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- Why do we need to add “COLD” alcohol? What is the effect of the temperature of the alcohol in the process of extracting the DNA.arrow_forwardIf you wanted to create recombinant DNA using this enzyme(3' T A 5'), would you have to cut both samples of DNA with this enzyme, or could you use two different restriction enzymes? Explain.arrow_forwardConsider the following: Restriction enzymes bind and cut between bases T and A. Based on this, which of the following are not acceptable VNTR segments? The DNA segment under consideration is AGTTAC GTTACA TCAATG CAATGTarrow_forward
- What are the major differences between dna probe and Primerarrow_forwardWhat is used to identify the size of a DNA molecule during gel electrophoresis?arrow_forwardWhat roles do restriction enzymes, vectors, and host cells play in recombinant DNA studies? What role does DNA ligase perform in a DNA cloning experiment? How does the action of DNA ligase differ from the function of restriction enzymes?arrow_forward
- When performing cloning experiments, it is not always necessary to treat sources of DNA with the same restriction enzyme. For example, DNA treated with EcoRI can be combined with DNA from a treatment using FunII. Explain why this is possible.arrow_forwardThe gene you are asked to clone is 30,000 bps in length. When you are choosing a suitable Restriction Endonuclease, what criteria about the enzyme can you deduce from the gene length?arrow_forwardExplain the role of the gene that is the selectable marker gene in this experiment.arrow_forward
- What is the dna strand sequence for phosphate sugar backbone? What are sticky ends in restriction enzymes can you examples to help me understand. Does where you cleave affect the length of the sticky ends overhang? 5-3directionalytgg atc gat atc gcc aat.arrow_forwardIn PCR amplification Why is it important to know the length of the sequence you amplify?arrow_forwardDuring PCR amplification in preparation for DNA sequencing, why were there different colors at the 3’ ends of the fragments produced? (What did these four colors represent?)arrow_forward
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