Team:BYU Provo/Notebook/SmallPhage/Summerexp

From 2013.igem.org

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<font size="3" font face="Calibri"> Our goals for these two weeks were very clear. First, we need to generate enough mutagenized phage for the Phage Purification Team to work with. Second, we need to work on our modeling project. Hopefully, everything will work out well and we will have presentable data soon! As for our modeling project, we have decide to model phage plaque sizes against different variables, such as phage particle size and top agar concentration. We aim to generate a mathematical model that can be used both to optimize phage plaque size for research and characterize our mutant phage. </font>
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<font size="3" font face="Calibri"> Our goals for these two weeks were very clear. First, we need to generate enough mutagenized phage for the Phage Purification Team to work with. Second, we need to start our modeling project. Hopefully, everything will go according to plan and we will have presentable data soon! As for our modeling project, we have decide to model phage plaque sizes against different variables, such as phage particle size and top agar concentration. We aim to generate a mathematical model that can be used both to optimize phage plaque size for research and characterize our mutant phage. </font>
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Revision as of 06:47, 18 August 2013


Small Phage May - June Notebook



Overview
March-April
May-June
July-August
September-October

July 1 - July 15


A new term and a fresh start! During these two weeks, we performed two more rounds of mutagenesis. With every experiment, we were able to perfect our protocol. Although our results are still not satisfactory, we are getting close! Eventually, we discovered that our phage stock decreased in titer during its preservation inside the fridge. We will propagate our phage and try again!


Daily log

Experiment Listing


Spring1.JPG


July 16 - July 31


During these couple weeks, we tried another 2 rounds of mutagenesis. The 5th round didn't work well so we made some major adjustments for the 6th round of mutagenesis. We believe that we were successful in finally mutating the phage and are giving them to the phage purification team to run a cesium chloride gradient on them.


Daily log

Experiment Listing



Spring2.JPG


August 1 - August 16


Our goals for these two weeks were very clear. First, we need to generate enough mutagenized phage for the Phage Purification Team to work with. Second, we need to start our modeling project. Hopefully, everything will go according to plan and we will have presentable data soon! As for our modeling project, we have decide to model phage plaque sizes against different variables, such as phage particle size and top agar concentration. We aim to generate a mathematical model that can be used both to optimize phage plaque size for research and characterize our mutant phage.


Daily log

Experiment Listing



Spring3.JPG


August 17 - August 31


Add description!


Daily log

Experiment Listing



Spring4.JPG