Difference between revisions of "Part:BBa K2926006"
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==Plasmid Design== | ==Plasmid Design== | ||
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− | For the analysis and characterization of the SNR52 Promotor | + | For the analysis and characterization of the SNR52 Promotor |
− | in combiantion with the SUP4 Terminaror | + | in combiantion with the SUP4 Terminaror, |
− | mCherry | + | mCherry was cloned beteen them using Gibson Assembly. |
The SNR52 Promotor and SUP4 Terminator where optained as a gBlock from IDT. | The SNR52 Promotor and SUP4 Terminator where optained as a gBlock from IDT. | ||
</html> | </html> | ||
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We performed the analysis with <i>E. coli DH5α</i> as well as <i>S. cerevisiae</i> cultures. | We performed the analysis with <i>E. coli DH5α</i> as well as <i>S. cerevisiae</i> cultures. | ||
<br> | <br> | ||
− | See <a href=" | + | See <a href="https://parts.igem.org/Part:BBa_K2926003">here</a> for the characterization results. |
</html> | </html> | ||
Latest revision as of 03:22, 22 October 2019
SUP4 yeast terminator
Usage and Biology
SUP4 is a natural terminator of Saccharomyces cerevisiae, belonging to the SUP4 tRNATyr locus.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Contents
Plasmid Design
For the analysis and characterization of the SNR52 Promotor in combiantion with the SUP4 Terminaror, mCherry was cloned beteen them using Gibson Assembly. The SNR52 Promotor and SUP4 Terminator where optained as a gBlock from IDT.
Sequencing Results
The biobrick was analysed with Sanger Sequenceing to confirm its correct base sequence.
Characterisation
We created a new protocol for the calibration of mCherry measurements with TexasRed,
based on the standard iGEM protocoll for GFP fluorescence calibration,
We performed the analysis with E. coli DH5α as well as S. cerevisiae cultures.
See here for the characterization results.
References