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Team:BYU Provo/Notebook/SmallPhage/Fallexp
From 2013.igem.org
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| - | <font size="3" font face="Calibri"> | + | <font size="3" font face="Calibri"> While the phage purification team was working out a kink in their cesium chloride gradient, we focused on modeling the relationship between capsid size and plaque size. Then once the cesium chloride gradient was perfected, we performed another round of mutagenesis, hoping that we would now be able to see mutant T7 bacteriophage. </font> |
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| - | <font size="3" font face="Calibri"> | + | <font size="3" font face="Calibri"> All our hard work finally paid off! We managed to isolate a smaller and a larger T7 bacteriophage! </font> |
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[[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/Period2/Dailylog|Daily log]] | [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/Period2/Dailylog|Daily log]] | ||
| - | [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/ | + | </font> |
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| + | | style="width: 20%; background-color: transparent;"| [[File:BYUSPFall2.JPG|220px|center|link=]] | ||
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| + | | <font size="5" font face="Calibri"> '''October 1 - October 15''' </font> | ||
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| + | <font size="3" font face="Calibri"> We had a great time at the iGEM regionals in Toronto! We're excited to be going to the World Championship Jamboree and got right back to work. Our first focus was getting good pictures of our mutant phage so that we could confirm their phenotypes. </font> | ||
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| + | <font color="#333399" size="4" font face="Calibri"> | ||
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| + | [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/Period3/Dailylog|Daily log]] | ||
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| + | [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/Period3/Explist|Experiment Listing]] | ||
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| + | | <font size="5" font face="Calibri"> '''October 16 - October 31''' </font> | ||
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| + | <br> | ||
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| + | <font size="3" font face="Calibri"> For the last weeks of iGEM, we continued to characterize the mutant phage more. We sequenced the capsid protein and searched for mutations. In addition, we cloned in the capsid proteins for T7 wild type, S4 (Small mutant 1), S10 (Small mutant 2), and L8 (Large Mutant 1). </font> | ||
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| + | <font color="#333399" size="4" font face="Calibri"> | ||
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| + | [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/Period4/Dailylog|Daily log]] | ||
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| + | [[Team:BYU_Provo/Notebook/SmallPhage/Fallexp/Period4/Explist|Experiment Listing]] | ||
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| + | </font> | ||
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| + | | style="width: 20%; background-color: transparent;"| [[File:asdfsa2.JPG|220px|center]] | ||
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Latest revision as of 03:27, 29 October 2013
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September 1 - September 15
While the phage purification team was working out a kink in their cesium chloride gradient, we focused on modeling the relationship between capsid size and plaque size. Then once the cesium chloride gradient was perfected, we performed another round of mutagenesis, hoping that we would now be able to see mutant T7 bacteriophage.
| 
|
| September 16 - September 30
All our hard work finally paid off! We managed to isolate a smaller and a larger T7 bacteriophage!
|  | |
| October 1 - October 15
We had a great time at the iGEM regionals in Toronto! We're excited to be going to the World Championship Jamboree and got right back to work. Our first focus was getting good pictures of our mutant phage so that we could confirm their phenotypes.
| File:Asdfsa1.JPG
| |
| October 16 - October 31
For the last weeks of iGEM, we continued to characterize the mutant phage more. We sequenced the capsid protein and searched for mutations. In addition, we cloned in the capsid proteins for T7 wild type, S4 (Small mutant 1), S10 (Small mutant 2), and L8 (Large Mutant 1).
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