Team:BYU Provo/Notebook/Phage Purification/Springexp

From 2013.igem.org

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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"> This semester we will are perfecting our procedures of purifying T4 and T7 bacteriophage through use of PEG and a CsCl gradient. </font>
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Revision as of 22:09, 7 June 2013


Phage Purification May - June Notebook



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

May 1 - May 12


This semester we will are perfecting our procedures of purifying T4 and T7 bacteriophage through use of PEG and a CsCl gradient.


Daily log

Experiment Listing

Progress Report


Spring1.JPG


May 13 - May 26


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!


Daily log

Experiment Listing

Progress Report



Spring2.JPG


May 27 - June 9


We finished our CsCl gradient and have started a new round of phage purification to run through the CsCl gradient again.


Daily log

Experiment Listing

Progress Report



Spring3.JPG


June 10 - June 23


Add description!


Daily log

Experiment Listing

Progress Report



Spring4.JPG
June 24 - June 30


Add description!


Daily log

Experiment Listing

Progress Report



Winter2.JPG