"
Team:Uppsala University/Results
From 2012.igem.org
(Difference between revisions)
| (15 intermediate revisions not shown) | |||
| Line 13: | Line 13: | ||
<div id="headlines"> | <div id="headlines"> | ||
| - | <a href=" | + | <a href="https://2012.igem.org/Team:Uppsala_University/Translational">sRNA Genes Silencing</a> | <a href="https://2012.igem.org/Team:Uppsala_University/Backbones">New standard backbone series</a> | <a href="https://2012.igem.org/Team:Uppsala_University/Promoters">Promoter characterization</a> | <a href="https://2012.igem.org/Team:Uppsala_University/Chromoproteins">Chromoproteins</a> | <a href="https://2012.igem.org/Team:Uppsala_University/catsac">Scarless Gene Deletion</a> |
</div> | </div> | ||
</div> | </div> | ||
| Line 24: | Line 24: | ||
<h2>sRNA gene silencing</h2> | <h2>sRNA gene silencing</h2> | ||
<div id="desc"> | <div id="desc"> | ||
| - | <p>We have developed a modular screening system and protocol for finding silencing | + | <p>We have developed a modular screening system and protocol for finding silencing sRNAs against arbitrary genes. Using this, we have found strongly silencing sRNAs against a clinical antibiotic gene and lowered the minimal inhibatory concentration ten-fold in resistant bacteria. |
</p> | </p> | ||
| - | <p><a href=" | + | <p id="more"><a href="/Team:Uppsala_University/Translational">Read more...</a> |
</div> | </div> | ||
</td> | </td> | ||
<td valign="top"> | <td valign="top"> | ||
| - | <img id="topimage" src="https://static.igem.org/mediawiki/2012/ | + | <img id="topimage" src="https://static.igem.org/mediawiki/2012/0/05/PEL4X15_temp.png" height="120"> |
<h2>New standard backbone series</h2> | <h2>New standard backbone series</h2> | ||
<div id="desc"> | <div id="desc"> | ||
| - | <p>We have constructed a range of new standard | + | <p>We have constructed a range of new standard low copy backbones, and variants with built-in lacIq repression for tight control of toxic genes, thermosensitivity and FRT sites for removing resistance cassettes. This work was as it turned out that the common registry pSB4 backbones all have faulty copy number regulation, while we needed low copy backbones for out project.</p> |
| + | <p id="more"><a href="/Team:Uppsala_University/Backbones">Read more...</a></p> | ||
</div> | </div> | ||
</td> | </td> | ||
| Line 63: | Line 64: | ||
<h2>Promoter characterization</h2> | <h2>Promoter characterization</h2> | ||
<div id="desc"> | <div id="desc"> | ||
| - | <p id="second">We have characterized promoter strengths of | + | <p id="second">We have characterized promoter strengths of eight popular promoters with Fluorescense Activated Cell Sorting (FACS), putting syntetic and wild-type promoters on the same scale. </p> |
| - | <p id="more"><a href="/Team:Uppsala_University/Promoters"> | + | <p id="more"><a href="/Team:Uppsala_University/Promoters">Read more...</a></div> |
</td> | </td> | ||
<td style="vertical-align: top"> | <td style="vertical-align: top"> | ||
<h2>Chromoproteins</h2> | <h2>Chromoproteins</h2> | ||
<div id="desc"> | <div id="desc"> | ||
| - | <p id="second">Proteins with | + | <p id="second">Proteins with a visible intrinsic color are the simplest possible reporters i molecular biology. Most iGEMers are familiar with the Red Flourescent Protein (RFP), but there are many other colors available among the organisms of the world. We have characterized and submitted new chromoproteins, allowing multiplexed colorful reporters. </p> |
| - | <p id="more"><a href="/Team:Uppsala_University/Chromoproteins"> | + | <p id="more"><a href="/Team:Uppsala_University/Chromoproteins">Read more...</a></div> |
</td> | </td> | ||
<td style="vertical-align: top"> | <td style="vertical-align: top"> | ||
<h2>Scarless gene deletion</h2> | <h2>Scarless gene deletion</h2> | ||
<div id="desc"> | <div id="desc"> | ||
| - | <p id="second">In our project we have extensivly used recombineering | + | <p id="second">In our project we have extensivly used homology recombineering into the bacterial chromosome. To aid this work, we have built a improved Cat-SacB selection-counterselection casette, which provides easy and reliable recombineering, and the possibility of scarless gene deletion. </p> |
| + | <p id="more"><a href="/Team:Uppsala_University/Catsac">Read more...</a></div> | ||
</td> | </td> | ||
</tr> | </tr> | ||
Latest revision as of 02:25, 27 October 2012
Facebook
Twitter
Blog (in Swedish)
EmailResults
sRNA gene silencingWe have developed a modular screening system and protocol for finding silencing sRNAs against arbitrary genes. Using this, we have found strongly silencing sRNAs against a clinical antibiotic gene and lowered the minimal inhibatory concentration ten-fold in resistant bacteria. |
New standard backbone seriesWe have constructed a range of new standard low copy backbones, and variants with built-in lacIq repression for tight control of toxic genes, thermosensitivity and FRT sites for removing resistance cassettes. This work was as it turned out that the common registry pSB4 backbones all have faulty copy number regulation, while we needed low copy backbones for out project. |
|
|
|
|
Promoter characterizationWe have characterized promoter strengths of eight popular promoters with Fluorescense Activated Cell Sorting (FACS), putting syntetic and wild-type promoters on the same scale. |
ChromoproteinsProteins with a visible intrinsic color are the simplest possible reporters i molecular biology. Most iGEMers are familiar with the Red Flourescent Protein (RFP), but there are many other colors available among the organisms of the world. We have characterized and submitted new chromoproteins, allowing multiplexed colorful reporters. |
Scarless gene deletionIn our project we have extensivly used homology recombineering into the bacterial chromosome. To aid this work, we have built a improved Cat-SacB selection-counterselection casette, which provides easy and reliable recombineering, and the possibility of scarless gene deletion. |
