Difference between revisions of "Part:BBa E0840"
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<b>New parts:</b> <partinfo>K1890020</partinfo>, <partinfo>K1890021</partinfo>, <partinfo>K1890022</partinfo>, <partinfo>K1890023</partinfo>, <partinfo>K1890024</partinfo>. | <b>New parts:</b> <partinfo>K1890020</partinfo>, <partinfo>K1890021</partinfo>, <partinfo>K1890022</partinfo>, <partinfo>K1890023</partinfo>, <partinfo>K1890024</partinfo>. | ||
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+ | <p><b>Characterization</b> | ||
Revision as of 20:15, 18 October 2016
GFP generator
BBa_E0840 takes as input a transcriptional signal (PoPS) and produce as output the fluorescent protein GFP.
Usage and Biology
- See BBa_E0040 for additional details.
- BBa_E0840 is often used to quantify the behavior of transcriptional control devices such as promoters.
- BBa_E0840 has a strong ribosome binding site.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 665
Improvements
Group: TU Delft 2016
Author: Lycka Kamoen and María Vázquez Vitali
Summary: Part BBa_E0840 does not contain any promoter, thus it can only be used if cloned downstream of one. It is also for this reason that this part (BBa_E0840) did not have any characterization. We have improved this BioBrick in 2 different ways: on the one hand, we provided 5 ready-to-go expression devices for green fluorescence (with promoters of different strengths), which can be used by future teams; on the other hand, this has allowed us to provide characterization for this uncharacterized GFP part. Using PCR primers, we added either of the constitutive promoters BBa_J23100, BBa_J23108, BBa_J23105, BBa_J23117 and BBa_J23113 to this part, to create five new biobrick devices. All of these biobricks were characterized by measuring their spectrum and growth cycle.New parts: BBa_K1890020, BBa_K1890021, BBa_K1890022, BBa_K1890023, BBa_K1890024.
Characterization