Team:Baltimore US/Notebook
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Notebook
June 7, 2010
Tom greeted us with 4 separate sheets that contained 3 reactions each for us to begin restrictions and began heating to let the enzymes cut. A lesson in what not to do, was offered as we began the heating cycle of restriction in the PCR blocks and he timing had been set to 35 seconds instead of 35 minutes, after which it heated to a kill cycle of 80 degrees and we had to reapply the enzymes, in case the enzymes had been denatured.
We had 6 individuals building the 4 sheets, 2 in redundancy.
The legend for the various parts is as follows...
1PO | BBa_R0063 |
2PO | BBa_P0412 |
3PO | pSBIT3 |
R (black marker) | BBa_R0062 |
I (black marker) | BBa_I13507 |
S (black marker) | pSBIT3 |
F (green marker) | BBa_F2620 |
I (green marker) | BBa_I13507 |
S (green marker) | pSBIC3 |
R10 (green marker) | BBa_R0010 |
462 (green marker) | BBa_I0462 |
IT3 (green marker) | pSBIT3 |
A/R10 (green marker) | BBa_R0010 |
B/462 (green marker) | BBa_I0462 |
C/IT3 (green marker) | pSBIT3 |
Patrick cut parts BBa_r0063 and BBa_p0412, and the plasmid backbone pSBIT3. The next step is to ligate them. Robert cut parts BBa_R0062 and BBa_I13507, and the plasmid backbone pSBIT3. Collin/Miles cut parts BBa_F2620, BBa_I13507 and the plasmid backbone pSBIC3 (labeled w/green marker).
After which we had a round table discussion about what kind of projects we may follow up with and the process of using the ncbi databases to discover pre-existing sequence information related to our various ideas. One idea we have discussed was the option of creating a smoother introductory curve for fellow DIY commmunity members and the creation of home-brewed enzymes that might be to pricey for the amateur scientists. We ended the night with the beginning of the various ligation reactions, as seen above.
- Ligstion Reaction for R10+462+IT3 in 'LIGATE 05X
- Ligstion Reaction for A/R10+B/462+C/IT3 in 'L/LIG