"
Team:TMU-Tokyo/Notebook
From 2012.igem.org
| Line 59: | Line 59: | ||
</p> | </p> | ||
<Br> | <Br> | ||
| + | <Center> | ||
| + | <IMG Src="https://static.igem.org/mediawiki/2012/9/92/Tmunotebook.JPG" align="right"></Center> | ||
| + | |||
<p class="description"> | <p class="description"> | ||
We described detail about experiment, protocols, and assay.<Br> | We described detail about experiment, protocols, and assay.<Br> | ||
| - | <Br> | + | <Br><Br><Br><Br><Br><Br><Br> |
<Br> | <Br> | ||
<b>■Experiment</b><Br> | <b>■Experiment</b><Br> | ||
| Line 73: | Line 76: | ||
<b>■Assay</b><Br> | <b>■Assay</b><Br> | ||
In order to confirm synthesized devices, we experimented functions of the devices using <i>Escherichia coli</i> transformed by plasmids inserted our devices. | In order to confirm synthesized devices, we experimented functions of the devices using <i>Escherichia coli</i> transformed by plasmids inserted our devices. | ||
| - | + | <Br> | |
| + | <Br> | ||
| + | <Br> | ||
| + | <Br> | ||
</div> | </div> | ||
Revision as of 19:24, 25 September 2012
■Experiment
1st week (8.13 - 8.19)
2nd week (8.20 - 8.26)
3rd week (8.27 - 9. 2)
4th week (9. 3 - 9. 9)
5th week (9.10 - 9.16)
6th week (9.17 - 9.23)
7th week (9.24 - 9.30)
■Protocols
Plasmid DNA Pure
Genome DNA Purification
Restruction Purification
DNA Fragment Ligation
Transformation
Electrophoresis
LB Medium
■Assay
Device1 Assay
Device2 Assay
Device3 Assay
Notebook
We described detail about experiment, protocols, and assay.
■Experiment
Genetic recombination experiment we did is described. We divided the experiment plan to parts completion and some teams concentrated on allocated experiments.
■Protocols
We crated own protocols with reference to the previous experiments last year, researching both inside and outside the team. Additionally, we improve the researched protocols through our experiments. So our protocols described here is really reliable. It must be useful in your experiments.
■Assay
In order to confirm synthesized devices, we experimented functions of the devices using Escherichia coli transformed by plasmids inserted our devices.
