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Team:Macquarie Australia/trial
From 2012.igem.org
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<p> With the break between semesters over the Macquarie iGEM returned to classes. For us this was the first day of iGEM 2012. We had our first meeting and discussed our project. Dr. Louise Brown and Associate Professor Rob Willows were introduced the team and we were began to determine who would take on certain roles within the team. </p> | <p> With the break between semesters over the Macquarie iGEM returned to classes. For us this was the first day of iGEM 2012. We had our first meeting and discussed our project. Dr. Louise Brown and Associate Professor Rob Willows were introduced the team and we were began to determine who would take on certain roles within the team. </p> | ||
| - | <p> | + | <p> We eagerly began our project, deciding to use the novel approach of Gibson Cloning. We had decided to develop a gene-switch controlled by light. To do this a couple of genes would be needed: |
<ol> | <ol> | ||
<li>a bacteriophytochrome</li> | <li>a bacteriophytochrome</li> | ||
Revision as of 10:01, 15 September 2012
To browse through our notebook simply click on the image with the date. It will expand with what we did that week. To continue on simply click on the next one.
With the break between semesters over the Macquarie iGEM returned to classes. For us this was the first day of iGEM 2012. We had our first meeting and discussed our project. Dr. Louise Brown and Associate Professor Rob Willows were introduced the team and we were began to determine who would take on certain roles within the team.
We eagerly began our project, deciding to use the novel approach of Gibson Cloning. We had decided to develop a gene-switch controlled by light. To do this a couple of genes would be needed:
- a bacteriophytochrome
- Heme oxygenase
The bacteriophytochromes from Deinococcus radiodurans and Agrobacterium tumefaciens were chosen. Over the next week Matt Stclair started to develop the G-blocks by:
- Acquiring the DNA sequence
- Translating into the protein sequence
- Using the DNA sequence, optimise codon usage for E. coli
- Translating into protein sequence and ensuring no changes in amino acids relative to the original sequence
Our lab work began today with the preparation of liquid media, plates and buffers. The protocols we followed are located here.
We prepared the following:
- Liquid LB Media
- SOC Solution
- SOB Solution
- LB Agar Plates
- Ampicillin LB Agar Plates: 31 plates
- Chloramphenicol LB Agar Plates: 33 Plates
- Kanamyacin LB Agar Plates: 32 Plates
- TB buffer.
- TAE buffer.
- EDTA buffer.
Ellaina, Matt Smith, Matt Stclair, Harry, Gazelle, Silas, Kim, and Miguel all worked on designing our G Blocks. Matt Stclair spearheaded the effort and proofread all the sequences we had developed.
This is a trial. I do not know if this is going to work or not!
This is a trial. I do not know if this is going to work or not!
This is a trial. I do not know if this is going to work or not!
This is a trial. I do not know if this is going to work or not!
This is a trial. I do not know if this is going to work or not!
This is a trial. I do not know if this is going to work or not!
This is a trial. I do not know if this is going to work or not!
