Difference between revisions of "Part:BBa K4806108"

 
Line 3: Line 3:
 
<partinfo>BBa_K4806108 short</partinfo>
 
<partinfo>BBa_K4806108 short</partinfo>
  
−
a
 
  
−
<!-- Add more about the biology of this part here
+
<html>
−
===Usage and Biology===
+
<style>
 +
    .bild {max-width: 100% ; height: auto;}
 +
    .unterschrift {font-size: 11.5px;}
 +
    .agarose {max-width: 700px; height: auto;}
 +
</style>
  
−
<!-- -->
 
−
<span class='h3bb'>Sequence and Features</span>
 
−
<partinfo>BBa_K4806108 SequenceAndFeatures</partinfo>
 
  
 +
<p>This level 1 composite part contains the AβSAP(i)-promotor (<a href=" https://parts.igem.org/Part:BBa_K4806013">BBa_K4806013</a>), the coding sequence of CYPCamC (<a href=" https://parts.igem.org/Part:BBa_K4806002">BBa_K4806002</a>), the HA-tag (<a href=" https://parts.igem.org/Part:BBa_K3002017">BBa_K3002017</a>)<sup>*</sup> for detection and the tRPL23-terminator (<a href="https://parts.igem.org/Part:BBa_K3002006">BBa_K3002006</a>)<sup>*</sup>. This part is codon-optimized for <i>Chlamydomonas reinhardtii</i> and was built as part of the CYPurify Collection.</p>
 +
<br>
 +
<h2>Construct</h2>
 +
<p>
 +
  <img class="bild" src="https://static.igem.wiki/teams/4806/wiki/registry/level2/cyp2d6-ha-construct.png">
 +
  <div class="unterschrift"><b>Fig.1 Construct design</b><br>
 +
  This construct was designed using the modular cloning system (MoClo).</div>
 +
</p>
 +
 
 +
<p><br></p>
 +
 +
<h2>Sequence and Features</h2>
 +
</html>
 +
<partinfo>BBa_K4806108 SequenceAndFeatures</partinfo>
  
−
<!-- Uncomment this to enable Functional Parameter display
 
−
===Functional Parameters===
 
 
<partinfo>BBa_K4806108 parameters</partinfo>
 
<partinfo>BBa_K4806108 parameters</partinfo>
−
<!-- -->
+
 
 +
 
 +
<html>
 +
<h2>Results</h2>
 +
<p>We confirmed that this construct is built correctly via agarose gel electrophoresis.</p>
 +
<p>
 +
  <img class="agarose" src="https://static.igem.wiki/teams/4806/wiki/registry/level2/2d6-ha.png">
 +
  <div class="unterschrift"><b>Fig.2 Test digest of CYPCamC level 1 with HA-tag</b><br>
 +
We digested this level 2 MoClo part with the restriction enzymes <i>Not</i>I and <i>Bste</i>II.</div></p>
 +
<p>The test digest in Fig.2 was compared to an in-silico digest. Together with the sequencing results we were able to demonstrate that our construct was built correctly.</p>
 +
<p><br></p>
 +
<h2>Contribution</h2>
 +
<p>The <sup>*</sup> marked parts were not created by us. Our results can be found on the experience page of each part.</p>
 +
</html>

Revision as of 09:59, 2 October 2023


CYPCamC gene with HA-tag for Chlamydomonas reinhardtii (Phytobrick)


This level 1 composite part contains the AβSAP(i)-promotor (BBa_K4806013), the coding sequence of CYPCamC (BBa_K4806002), the HA-tag (BBa_K3002017)* for detection and the tRPL23-terminator (BBa_K3002006)*. This part is codon-optimized for Chlamydomonas reinhardtii and was built as part of the CYPurify Collection.


Construct

Fig.1 Construct design
This construct was designed using the modular cloning system (MoClo).


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1023
    Illegal PstI site found at 1295
    Illegal PstI site found at 2019
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 249
    Illegal PstI site found at 1023
    Illegal PstI site found at 1295
    Illegal PstI site found at 2019
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 530
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1023
    Illegal PstI site found at 1295
    Illegal PstI site found at 2019
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1023
    Illegal PstI site found at 1295
    Illegal PstI site found at 2019
    Illegal NgoMIV site found at 3040
    Illegal AgeI site found at 268
  • 1000
    COMPATIBLE WITH RFC[1000]


Results

We confirmed that this construct is built correctly via agarose gel electrophoresis.

Fig.2 Test digest of CYPCamC level 1 with HA-tag
We digested this level 2 MoClo part with the restriction enzymes NotI and BsteII.

The test digest in Fig.2 was compared to an in-silico digest. Together with the sequencing results we were able to demonstrate that our construct was built correctly.


Contribution

The * marked parts were not created by us. Our results can be found on the experience page of each part.