Difference between revisions of "Team:Freiburg/Project/pRIG15 11"
(6 intermediate revisions by 2 users not shown) | |||
Line 4: | Line 4: | ||
{{Freiburg/wiki_content_start}} | {{Freiburg/wiki_content_start}} | ||
<html> | <html> | ||
+ | |||
+ | <!--========= BEGIN: GoBack button ==========--> | ||
+ | <div class="button_back"> | ||
+ | <a style="color:#FFF" href="https://2015.igem.org/Team:Freiburg/Parts"> << Back</a> | ||
+ | </div> | ||
+ | <!--========= END: GoBack button ==========--> | ||
+ | |||
+ | <style> | ||
+ | /*========= BEGIN: style for navigation bar ==========*/ | ||
+ | #results { | ||
+ | background: url(https://static.igem.org/mediawiki/2015/2/2e/Freiburg_icon_results_active_yellow.png) no-repeat; | ||
+ | } | ||
+ | |||
+ | #results a { | ||
+ | color: #ecdc18; | ||
+ | } | ||
+ | |||
+ | #runningchip { | ||
+ | left: 52%; | ||
+ | } | ||
+ | /*========= END: style for navigation bar ==========*/ | ||
+ | </style> | ||
+ | |||
<!-- Labjournal content goes in here --> | <!-- Labjournal content goes in here --> | ||
<div class="content_box"> | <div class="content_box"> | ||
Line 24: | Line 47: | ||
<p> | <p> | ||
− | The bacterium <a class="wikilink1" href="https://2015.igem.org/Team:Freiburg/Project/Diseases#Tetanus" title="Tetanus">< | + | The bacterium <a class="wikilink1" href="https://2015.igem.org/Team:Freiburg/Project/Diseases#Tetanus" title="Tetanus"><i>Clostridum tetani</i></a> can cause severe illness due to its neurotoxin which causes strong muscular spasms eventual leading to death. For our experiments we decided to use a sequence which codes for the carboxyl fragment of the heavy chain of tetanus neurotoxin. Although this part is derived from the neurotoxin it is not pathogenic itself.<sup><a class="fn_top" href="#fn__1" id="fnt__1" name="fnt__1">1)</a></sup> |
</p> | </p> | ||
<p> | <p> | ||
− | To insert the sequence for TeNT_Hc into pSB1C3 we designed Gibson primers with compatible overhangs that also included the start codon ATG. This fragment was amplified via <a class="wikilink1" href="https://2015.igem.org/Team:Freiburg/Labjournals/Cloning/August#PCRbb11" title="PCRbb11">PCR</a> and then assembled with the digested pSB1C3 backbone using Gibson assembly. | + | To insert the sequence for TeNT_Hc into <a class="urlextern" href="http://parts.igem.org/Part:pSB1C3" target="_blank" title="pSB1C3">pSB1C3</a> we designed Gibson primers with compatible overhangs that also included the start codon ATG. This fragment was amplified via <a class="wikilink1" href="https://2015.igem.org/Team:Freiburg/Labjournals/Cloning/August#PCRbb11" title="PCRbb11">PCR</a> and then assembled with the digested <a class="urlextern" href="http://parts.igem.org/Part:pSB1C3" target="_blank" title="pSB1C3">pSB1C3</a> backbone using Gibson assembly. |
To prove correct insertion of our fragment we did a <a class="wikilink1" href="https://2015.igem.org/Team:Freiburg/Labjournals/Cloning/August#TDbb11" title="TDbb11">test digest</a> and sent the whole plasmid for sequencing. | To prove correct insertion of our fragment we did a <a class="wikilink1" href="https://2015.igem.org/Team:Freiburg/Labjournals/Cloning/August#TDbb11" title="TDbb11">test digest</a> and sent the whole plasmid for sequencing. | ||
− | During our project we inserted the sequence coding for TeNT_Hc into pET22b+ and induced overexpression of the protein in < | + | During our project we inserted the sequence coding for TeNT_Hc into pET22b+ and induced overexpression of the protein in <i>E.coli</i>. We could show successfull overexpression of TeNT_Hc (figure 2). As verification for our results we use a western blot (figure 3). |
Line 40: | Line 63: | ||
<div class="thumbcaption"> | <div class="thumbcaption"> | ||
</a> | </a> | ||
− | <p><strong>Figure 2: 12 | + | <p><strong>Figure 2: 12.5% SDS-PAGE analysis of the purification of <a href="http://parts.igem.org/Part:BBa_K1621003"><i>C. tetani</i> antigen</a>.</strong> Protein purification was performed with gravity flow columns and Ni-NTA Agarose. The protein was eluted by 500mM imidazole. The expected molecular weight is 50 kDa. FT-Flowthrough, W-Wash, E-Elution.</p> |
</div> | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
+ | </div> | ||
+ | <div class="image_box right"> | ||
<div class="thumb2 trien" style="width:310px"> | <div class="thumb2 trien" style="width:310px"> | ||
<div class="thumbinner"> | <div class="thumbinner"> | ||
Line 56: | Line 81: | ||
</div> | </div> | ||
− | + | </br></br></br></br></br></br></br></br></br></br></br></br></br></br></br></br></br> | |
− | + | Link to GeneBank file: <a class="media" href="https://static.igem.org/mediawiki/2015/e/ee/Freiburg_2015_BBa_K1621003.gb" title="2015_Freiburg_BBa_K1621003" src="https://static.igem.org/mediawiki/2015/e/ee/Freiburg_2015_BBa_K1621003.gb">BBa_K1621003.gb</a>. | |
+ | </br> | ||
+ | Link to Registry: <a href="http://parts.igem.org/Part:BBa_K1621003" target="_blank">BBa_K1621003</a> | ||
</div> | </div> |
Latest revision as of 23:18, 16 September 2015
![](https://static.igem.org/mediawiki/2015/8/85/Freiburg_wiki_background_2_parted_left.png)
![](https://static.igem.org/mediawiki/2015/f/f4/Freiburg_wiki_background_2_parted_right.png)
pRIG15_11
The bacterium Clostridum tetani can cause severe illness due to its neurotoxin which causes strong muscular spasms eventual leading to death. For our experiments we decided to use a sequence which codes for the carboxyl fragment of the heavy chain of tetanus neurotoxin. Although this part is derived from the neurotoxin it is not pathogenic itself.1)
To insert the sequence for TeNT_Hc into pSB1C3 we designed Gibson primers with compatible overhangs that also included the start codon ATG. This fragment was amplified via PCR and then assembled with the digested pSB1C3 backbone using Gibson assembly. To prove correct insertion of our fragment we did a test digest and sent the whole plasmid for sequencing. During our project we inserted the sequence coding for TeNT_Hc into pET22b+ and induced overexpression of the protein in E.coli. We could show successfull overexpression of TeNT_Hc (figure 2). As verification for our results we use a western blot (figure 3).