Difference between revisions of "Part:BBa K2054001"
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<img src="https://static.igem.org/mediawiki/parts/4/48/T--HK_SKHLPSS--HKU_assay2.png" alt="p1" style="width:40%"/> | <img src="https://static.igem.org/mediawiki/parts/4/48/T--HK_SKHLPSS--HKU_assay2.png" alt="p1" style="width:40%"/> | ||
<img src="https://static.igem.org/mediawiki/parts/a/a8/T--HK_SKHLPSS--HKU_assay3.png" alt="p1" style="width:40%"/> | <img src="https://static.igem.org/mediawiki/parts/a/a8/T--HK_SKHLPSS--HKU_assay3.png" alt="p1" style="width:40%"/> | ||
| + | </html> | ||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K2054001 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2054001 SequenceAndFeatures</partinfo> | ||
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Revision as of 10:37, 21 October 2019
Oligo 1
This will be use to build our desired nanostructure. This ssDNA contains also split G-quadruplex sequences that allow the oligo itself to function as an DNAzyme under specific conditions.
Usage and Biology
- Group: Team: HK_SKHLPSS, 2019
- Author: Tse Cheong Tat
- Summary: The peroxidase activity of the nano-structure formed from parts BBa_K2054001and BBa_K2054005 were measured. It was found that the nano-structure formed from these two parts had a high specificity in detecting the target sequence, showing that the purified ssDNAs produced from plasmid could work as per their design and function well. Details of our experimental characterization could be found on here.
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Relevant documentation:
Sequence and Features
Assembly Compatibility: