I think overall this presentation is very well organized and presented and I liked how in depth you explained each section. I also like the way you presented the data and presented every aspect of it. Great job!
This was a great project, I really appreciated the background on what bacteriophages are and how they work in bacteria. I am curious about what qualifies DNA as high quality in a PCR gel?
You presented your poster well and spoke clearly. The background of the experiment, results, and conclusions are well understood. How did you determine your future directions after your results?
we determine our future directions because since it is a lytic phage, we could then see which diseases can be target using lytic phages, but further tests would be necessary.
Thanks for sharing your research! It was great to see how you isolated your phage on the CU campus! How exactly did you do that? Also, how did you know it belonged to phage cluster A versus another cluster? Lastly, what was in your DNA ladder for Figures 3 and 4?
we know it belong to Cluster A because of the restriction digest gel which with the results gotten from that, you compare it to others ones’ and depending on which is more similar it is the one the it belongs too.
We knew it belong to this cluster because of the restriction digest gel, which depending on the results you got, you put your information at a website, and it compares it to others and they would tell you to which one it belongs to.
curesymposium.org 
I think overall this presentation is very well organized and presented and I liked how in depth you explained each section. I also like the way you presented the data and presented every aspect of it. Great job!
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This was a great project, I really appreciated the background on what bacteriophages are and how they work in bacteria. I am curious about what qualifies DNA as high quality in a PCR gel?
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for being qualified as high quality, it should display bright concentrated bands with no streaks.
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You presented your poster well and spoke clearly. The background of the experiment, results, and conclusions are well understood. How did you determine your future directions after your results?
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we determine our future directions because since it is a lytic phage, we could then see which diseases can be target using lytic phages, but further tests would be necessary.
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Good job! What are the negative consequences to phage therapy, if any?
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A possible risk of phage therapy is that phage inserts its DNA into the host cells
body cell genomes.
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Thanks for sharing your research! It was great to see how you isolated your phage on the CU campus! How exactly did you do that? Also, how did you know it belonged to phage cluster A versus another cluster? Lastly, what was in your DNA ladder for Figures 3 and 4?
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we know it belong to Cluster A because of the restriction digest gel which with the results gotten from that, you compare it to others ones’ and depending on which is more similar it is the one the it belongs too.
LikeLike
We knew it belong to this cluster because of the restriction digest gel, which depending on the results you got, you put your information at a website, and it compares it to others and they would tell you to which one it belongs to.
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Good job on the presentation! What were the methods you used to determine each of the results?
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