Difference between revisions of "Part:BBa K2201207:Design"
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The coding sequence of the synthetase has to be inserted into a linearized ONBY-Part. For example per Gibson Assembly of a gene synthesis with matching overahangs. | The coding sequence of the synthetase has to be inserted into a linearized ONBY-Part. For example per Gibson Assembly of a gene synthesis with matching overahangs. | ||
+ | It can be obtained by cloning the CDS in the linearized ONBY-part as shown in <b>Figure 1</b>. | ||
+ | [[File:T--Bielefeld-CeBiTec--YKE_AzoF_RS_History1.png|thumb|600px|center| <b>Figure 1:</b> History of the plasmid construction of K2201207.]] | ||
===Source=== | ===Source=== |
Latest revision as of 16:23, 1 November 2017
Expression plasmid of an aminoacyl-tRNA synthetase for AzoPhe
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1164
Illegal BamHI site found at 1170 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1196
Illegal NgoMIV site found at 1656 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 295
Illegal SapI.rc site found at 327
Illegal SapI.rc site found at 1120
Design Notes
The coding sequence of the synthetase has to be inserted into a linearized ONBY-Part. For example per Gibson Assembly of a gene synthesis with matching overahangs.
It can be obtained by cloning the CDS in the linearized ONBY-part as shown in Figure 1.
Source
Collaboration with CU Boulder, Schultz lab, Addgene