Unit 6 Reflection

This unit's main topics were biotechnology and bioethics. We also learned about recombinant DNA, PCR, electrophoresis, and sequencing. Biotechnology is the study and manipulation of living things including their molecules, cells, tissues, or organs in order to benefit mankind. Bioethics is the study of decision making as it applies to moral decisions that have to be made because of advances in biology, medicine, and technology. A main theme of this unit was that recombinant DNA is the insertion of one organism's DNA into the DNA is another organism. It is similar to generic engineering and the result of recombinant DNA technology is a transgenic organism, or GMO. Another essential understanding of this unit is that electricity is used to separate DNA fragments based on size in a process called gel electrophoresis. Larger fragments of DNA travel less and move slower than smaller fragments. Other main ideas of this unit include using sequencing to determine the exact order of a DNA strand and using DNA Polymerase, primers, extra bases, and florescent dyes to create copies of them. A strength that I had in this unit was understanding gel electrophoresis well and knowing exactly how the process works. However, a weakness that I had was having trouble understanding the pGLO lab and the reasons why bacteria grew in some places and didn't in other places. A success that I had was knowing some real life applications of PCR, or Polymerase Chain Reaction before we learned about them. I knew that PCR can be used for paternity testing, detecting diseases, and conducting forensic investigations. A setback that I have is not knowing some of the steps for PCR and what exactly happens in each of them. For this unit we did the recombinant DNA  lab, the candy electrophoresis lab, and the pGLO lab. In the recombinant DNA lab we had to find the correct restriction enzyme that would cut the plasmid in one place and the human DNA in two places. In the candy electrophoresis lab, we took the dyes of different candies and compared them to some reference bands. We then ran the gel electrophoresis and looked at the results. In our pGLO lab, we took a variety of petri dishes and put bacteria in them. One petri dish had +pGLO with LB/amp/ara, another had -pGLO with LB, and so on. At the end we saw which of the petri dishes had bacteria in them and whether any one of them glowed. All these labs helped me further understand the concepts of this unit. I want to learn more in depth about electrophoresis and its applications. An unanswered question that I have is whether or not the genetic modification of human embryos is really in fact possible. I wonder about if our world will become like the world in the movie GATTACA. I think I am on track to fulfill my New Year's goals. I have been procrastinating less and getting more work done in class than before.