Difference between revisions of "Team:Glasgow/Project/Overview/Terminator"

Line 392: Line 392:
 
         <div class='containerRight'>
 
         <div class='containerRight'>
 
<h2 style="margin-top:13vh;">Summary</h2>
 
<h2 style="margin-top:13vh;">Summary</h2>
               <p class="mainText">Aim: To characterise K1725081 for submission to the registry.
+
               <p class="mainText">Aim: To characterise the T1 terminator from <i>E. coli rrnB</i>, K1725081, for submission to the registry.
 
</br>
 
</br>
 
</br>
 
</br>
Line 400: Line 400:
 
Basic Parts submitted:
 
Basic Parts submitted:
 
</br>
 
</br>
• <a href="http://parts.igem.org/Part:BBa_K1725081">BBa_K1725081</a> – T1 terminator from <i>E. coli</i> rrnB
+
• <a href="http://parts.igem.org/Part:BBa_K1725081">BBa_K1725081</a>
 
</br>
 
</br>
 
</br>
 
</br>
Line 425: Line 425:
 
</br>
 
</br>
 
</br>
 
</br>
 
<h2>Results</h2>
 
- Cell-cell comunication
 
</br>
 
- Decanal experiments
 
</br>
 
- Spectrum experiments and comparison to Cambridge operon
 
 
<div class="scrollConclusion"></div>
 
</br></br>
 
  
 
      
 
      

Revision as of 09:56, 17 September 2015

Glasglow

Terminator

Summary

Aim: To characterise the T1 terminator from E. coli rrnB, K1725081, for submission to the registry.

Results Overview: K1725081 was successful in terminating transcription to the same level as B0010 and B0015.

Basic Parts submitted:
BBa_K1725081



Introduction

text



Methods

text



text



Results

text


Conclusion

Location

Bower Building, Wilkins Teaching Laboratory
University of Glasgow
University Avenue
G12 8QQ

Follow Us On