Difference between revisions of "Part:BBa K4806108"
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<h2>Construct</h2> | <h2>Construct</h2> | ||
<p> | <p> | ||
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<div class="unterschrift"><b>Fig.1 Construct design</b><br> | <div class="unterschrift"><b>Fig.1 Construct design</b><br> | ||
This construct was designed using the modular cloning system (MoClo).</div> | This construct was designed using the modular cloning system (MoClo).</div> | ||
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<p>We confirmed that this construct is built correctly via agarose gel electrophoresis.</p> | <p>We confirmed that this construct is built correctly via agarose gel electrophoresis.</p> | ||
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<div class="unterschrift"><b>Fig.2 Test digest of CYPCamC level 1 with HA-tag</b><br> | <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> | We digested this level 2 MoClo part with the restriction enzymes <i>Not</i>I and <i>Bste</i>II.</div></p> |
Revision as of 10:33, 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
This construct was designed using the modular cloning system (MoClo).
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 1023
Illegal PstI site found at 1295
Illegal PstI site found at 2019 - 12INCOMPATIBLE 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 - 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 530
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 1023
Illegal PstI site found at 1295
Illegal PstI site found at 2019 - 25INCOMPATIBLE 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 - 1000COMPATIBLE WITH RFC[1000]
Results
We confirmed that this construct is built correctly via agarose gel electrophoresis.
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.