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Team:BYU Provo/Notebook/SmallPhage/Summerexp
From 2013.igem.org
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| - | | colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Small Phage | + | | colspan="3" | <font color="#333399" size="5" font face="Calibri"> |
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| + | : '''Small Phage July - August Notebook'''</font> | ||
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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="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 | + | <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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| - | <font size="3" font face="Calibri"> | + | <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/Summerexp/Period2/Explist|Experiment Listing]] | [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period2/Explist|Experiment Listing]] | ||
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| - | | <font size="5" font face="Calibri"> ''' | + | | <font size="5" font face="Calibri"> '''August 1 - August 16''' </font> |
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| - | <font size="3" font face="Calibri"> | + | <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/Summerexp/Period3/Explist|Experiment Listing]] | [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period3/Explist|Experiment Listing]] | ||
| - | + | </font> | |
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| - | | <font size="5" font face="Calibri"> ''' | + | | <font size="5" font face="Calibri"> '''August 17 - August 31''' </font> |
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| - | <font size="3" font face="Calibri"> | + | <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/Summerexp/Period4/Explist|Experiment Listing]] | [[Team:BYU_Provo/Notebook/SmallPhage/Summerexp/Period4/Explist|Experiment Listing]] | ||
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Latest revision as of 02:52, 28 September 2013
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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!
| 
|
| 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.
| 
| |
| 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.
| 
| |
| 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.
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