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Project/Venus/
From 2010.igem.org
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[[Image:Venus_digest.JPG]] <br /> <br /> | [[Image:Venus_digest.JPG]] <br /> <br /> | ||
| - | <br /> | + | The Venus fragment was ligated into the linearised form of PSB1C3 (digested with EcoR1 and Pst1) and the re-digested with EcoR1 and Pst1 so to confirm the successful ligation. <br /> |
| + | [[Image:Venus_in_PSB1C3.JPG]] <br /> <br /> | ||
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| + | The completed ligation of Venus into the PSB1C3 plasmid is depicted on the plasmid map (below) along with all annotations and landmark features [1]. <br /> | ||
| + | [[Image:Venus_plasmid_map.JPG]] <br /> | ||
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=== Testing and verification === | === Testing and verification === | ||
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Revision as of 10:41, 24 October 2010
Contents |
Characterisation of the fluorescent reporter protein - Venus - [http://partsregistry.org/Part:BBa_K354002 BBa_K354002]
BioBrick Background
Sequence Development and Annotation
As was the case in the assembly of the PlcR-PapR BioBrick, the synthesized Venus BioBrick was received in the pMK plasmid (below).
Once digested with EcoR1 and Pst1, the Venus fragment was recovered via gel extraction and purified in preparation for its ligation into PSB1C3. Lane 2 houses the Venus digest with the excised fragment shown (782bp).
The Venus fragment was ligated into the linearised form of PSB1C3 (digested with EcoR1 and Pst1) and the re-digested with EcoR1 and Pst1 so to confirm the successful ligation.
The completed ligation of Venus into the PSB1C3 plasmid is depicted on the plasmid map (below) along with all annotations and landmark features [1].
Testing and verification
