Team:TMU-Tokyo
From 2013.igem.org
Masashiohara (Talk | contribs) |
Masashiohara (Talk | contribs) |
||
Line 38: | Line 38: | ||
<table class="stand" rules="none" border="1" width="450" height="270"> | <table class="stand" rules="none" border="1" width="450" height="270"> | ||
<tr height="30"><td align="center"><b>Standardization</b></td></tr> | <tr height="30"><td align="center"><b>Standardization</b></td></tr> | ||
- | <tr height="200"><td style="padding:3px 7px;"><p>In order to insert Biobricks in to a genome of <i>E.coli</i> and functionalize them, we made a new and interesting method and standardize it. In this new method named “NEWS”, we constructed all of our parts by over rap extension PCR and inserted these PCR products in to a genome of <i>E.coli</i> by lambda bacteriophage recombination system, ”RED”. Also we designed a new parts which to improve the present designated vector. With this parts, it can be easily to do cloning the parts which made by PCR.<br> | + | <tr height="200"><td style="padding:3px 7px;"><p><a href="https://2013.igem.org/Team:TMU-Tokyo/Project/NEWS" style="text-decoration:none; color:#000;">In order to insert Biobricks in to a genome of <i>E.coli</i> and functionalize them, we made a new and interesting method and standardize it. In this new method named “NEWS”, we constructed all of our parts by over rap extension PCR and inserted these PCR products in to a genome of <i>E.coli</i> by lambda bacteriophage recombination system, ”RED”. Also we designed a new parts which to improve the present designated vector. With this parts, it can be easily to do cloning the parts which made by PCR.<br> |
<p>Additionally, we standardized this method so that other iGEMers could use it. So we’ll apply for New Standard prize.</p> | <p>Additionally, we standardized this method so that other iGEMers could use it. So we’ll apply for New Standard prize.</p> | ||
</td></tr> | </td></tr> |
Revision as of 12:30, 25 September 2013
In the iGEM, most teams have inserted their Biobrick parts or devices into the plasmids and use them. It is true that there are many good points to use plasmids, for instance, it is easy to do transformation, and it is convenient to use high copy plasmid when you want to get high gene expression amount. However, there are some bad points to use plasmids too. For example, when the reproduction starting point of plural plasmids are covered, it can’t put in E.coli at the same time. Also it is difficult to control genetic expression closely. Therefore, in this year, our team tried to standardize a new method to inserted Biobrick parts or devices in a genome of E.coli and used them. Also we really inserted the device which we designed in a genome of E.coli according to our method and functionalized it. |
|
|
|
|
|
|