Hi Neely. Our biggest issue was that we had to redo our PCR a few times and so we had limited time with it. We would have liked to run a PCR with the controls.
Hi Carlos. If it is found that the speed of lysis is to low genetic engineering could potentially be used to adjust the speed of lysis up to more useful levels.
Hello! Why the positive and negative controls were run on a different gel? Great job on the presentation!
Hi Madison. The controls were run on a different gel as a cost saving measure. As the class made only one set of controls per lab period.
Hi Jacob! Were there any limitations that you ran into while studying your phage?
Hi Neely. Our biggest issue was that we had to redo our PCR a few times and so we had limited time with it. We would have liked to run a PCR with the controls.
How can your siphoviridae phage be used for phage therapy if it is found that the speed of lysis is not at fast as other phages in the F1 family?
Hi Carlos. If it is found that the speed of lysis is to low genetic engineering could potentially be used to adjust the speed of lysis up to more useful levels.