Team:BYU Provo/Notebook/SmallPhage/Summerexp

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| colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Small Phage May - June Notebook'''</font>
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| colspan="3" | <font color="#333399" size="5" font face="Calibri">  
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: '''Small Phage July - August Notebook'''</font>
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: [[Team:BYU_Provo/Small_Phage|Overview]]
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: <u> '''Small Phage''' </u> </font>
: [[Team:BYU Provo/Notebook/SmallPhage/Winterexp|March-April]]
: [[Team:BYU Provo/Notebook/SmallPhage/Winterexp|March-April]]
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<font size="5" font face="Calibri"> '''May 1 - May 12''' </font>
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<font size="5" font face="Calibri"> '''July 1 - July 15''' </font>
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<font size="3" font face="Calibri"> This is the start of Spring Term at BYU! The weather is finally getting better: no more snowing. And we are ready to do some serious lab work! While we are waiting for our mutgen, 5-bromodeoxyuridine, to arrive, we decided to start this term with establishing the basic procedures for our direct evolution method. Specifically, this involves making sure that we can (1) grow and amplify T7 phage in liquid culture, (2) select for smaller phage using concentrated top agar, and (3) amplify phage from a single plaque. During these two weeks, we also designed primers for cloning and sequencing T7 capsid proteins as well as mapped out detailed procedures for both cloning T7 capsid proteins and applying mutagen. </font>
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<font size="3" font face="Calibri"> 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!</font>
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period1/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period1/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/PR| Progress Report]] </font>
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| style="width: 20%; background-color: transparent;"| [[File:Spring1.JPG|250px|center]]
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| <font size="5" font face="Calibri"> '''May 13 - May 26''' </font>
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| <font size="5" font face="Calibri"> '''July 16 - July 31''' </font>
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<font size="3" font face="Calibri"> In these two weeks, we performed our first round of mutagenesis and first PCR. Although we are still testing the results to optimize our protocol, we are optimistic about the outcome!</font>
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<font size="3" font face="Calibri"> 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. </font>
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period2/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period2/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period2/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period2/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period2/PR| Progress Report]] </font>
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| style="width: 20%; background-color: transparent;"| [[File:Spring2.JPG|250px|center]]
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| <font size="5" font face="Calibri"> '''May 27 - June 9''' </font>
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| <font size="5" font face="Calibri"> '''August 1 - August 16''' </font>
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<font size="3" font face="Calibri"> Add description! </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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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period3/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period3/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period3/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period3/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period3/PR| Progress Report]] </font>
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| <font size="5" font face="Calibri"> '''August 17 - August 31''' </font>
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<font size="3" font face="Calibri"> These two weeks are the interim between summer term and fall semester at BYU. During these two weeks, we focused mostly on finalizing our mutagenesis procedure with the help of Phage Purification Team and their CsCl gradient protocol. We completed our seventh round of mutagenesis and we did see a variability in the size of phage plaques indication variability in phage capsid size. We conducted the eighth round of mutagenesis even more meticulously. Toward the end of these two-week period, we are working on characterizing phage. From our preliminary data, we are seeing the most concentrated phage after mutagenesis so far, which is very promising. </font>
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period4/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period4/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period4/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period4/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period4/PR| Progress Report]] </font>
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period5/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period5/Explist|Experiment Listing]]
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[[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period5/PR| Progress Report]] </font>
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Latest revision as of 02:52, 28 September 2013


Small Phage July - August Notebook



Small Phage
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


Lsadjf.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



Ouawr.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



Nsdfj.JPG


August 17 - August 31


These two weeks are the interim between summer term and fall semester at BYU. During these two weeks, we focused mostly on finalizing our mutagenesis procedure with the help of Phage Purification Team and their CsCl gradient protocol. We completed our seventh round of mutagenesis and we did see a variability in the size of phage plaques indication variability in phage capsid size. We conducted the eighth round of mutagenesis even more meticulously. Toward the end of these two-week period, we are working on characterizing phage. From our preliminary data, we are seeing the most concentrated phage after mutagenesis so far, which is very promising.


Daily log

Experiment Listing



6Small.JPG