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Team:BYU Provo/Notebook/SmallPhage/Springexp
From 2013.igem.org
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Overview | Overview | ||
| - | Winter | + | [[Team:BYU Provo/Notebook/SmallPhage/Winterexp|Winter]] |
[[Team:BYU Provo/Notebook/SmallPhage/Springexp|Spring]] | [[Team:BYU Provo/Notebook/SmallPhage/Springexp|Spring]] | ||
| - | Summer | + | [[Team:BYU Provo/Notebook/SmallPhage/Summerexp|Summer]] |
| - | Fall | + | [[Team:BYU Provo/Notebook/SmallPhage/Fallexp|Fall]] |
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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> | <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 color="#333399" size="4" font face="Calibri"> | |
| - | + | [[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Dailylog|Daily log]] | |
| - | + | [[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Dailylog|Experiment Listing]] | |
| - | + | Progress Report </font> | |
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| + | : [[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Exp/Team:BYU_Provo/5.3 T7 phage selection method test|5.3 T7 phage selection method test]] | ||
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| + | : [[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Exp/Team:BYU_Provo/5.3 Phage Amplification/Purification|5.3 Phage Amplification/Purification]] | ||
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| + | </font> | ||
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| + | <font color="#333399" size="4" font face="Calibri"> | ||
| style="width: 20%; background-color: transparent;"| [[File:Spring1.JPG|250px|center]] | | style="width: 20%; background-color: transparent;"| [[File:Spring1.JPG|250px|center]] | ||
Revision as of 15:39, 27 May 2013
| Small Phage Spring Notebook
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Overview Spring
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April 29 - May 12
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.
Progress Report
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May 13 - May 26
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May 27 - June 9
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June 10 - June 23
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