Difference between revisions of "Part:BBa K2753055"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K2753055 short</partinfo> | <partinfo>BBa_K2753055 short</partinfo> | ||
− | The promoter UP119 is a modified variant of J23119 consensus promoter[[ | + | |
+ | The promoter UP119 is a modified variant of J23119 consensus promoter ([[Part:BBa_J23119]]) by adding an up-element. This alteration makes UP119 stronger than the original J23119. | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | |||
+ | <html> | ||
+ | <center> | ||
+ | <Figure> | ||
+ | <img width="70%" src="https://static.igem.org/mediawiki/2018/9/9e/T--GreatBay_China--119_design.png"> | ||
+ | </figure> | ||
+ | </center> | ||
+ | </html> | ||
+ | <br/> | ||
+ | |||
+ | <p>By changing the sequence of UP119 to create a binding site for TALE2, we obtained another J23119 variant and has made it the core promoter sequence of a member from the TALE stabilised promoter family, pTALE2 sp6.</p> | ||
+ | |||
+ | ===Characterisation in comparison to J23119=== | ||
+ | |||
+ | <!--表征图--> | ||
+ | |||
+ | <p>For comparing the strength of two J23119 variants with J23119, we cloned them with a sfGFP onto three plasmids of distinctive copy numbers.</p> | ||
+ | <ul> | ||
+ | <li>pUC20: ~500</li> | ||
+ | <li>pR6K: ~15</li> | ||
+ | <li>pSC101: ~1</li> | ||
+ | </ul> | ||
+ | <br> | ||
+ | <p>The strength of them are characterised by measuring the fluorescence using a Flow Cytometry.</p> | ||
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Latest revision as of 15:17, 13 October 2018
UPJ23119
The promoter UP119 is a modified variant of J23119 consensus promoter (Part:BBa_J23119) by adding an up-element. This alteration makes UP119 stronger than the original J23119.
For comparing the strength of two J23119 variants with J23119, we cloned them with a sfGFP onto three plasmids of distinctive copy numbers.
- pUC20: ~500
- pR6K: ~15
- pSC101: ~1
The strength of them are characterised by measuring the fluorescence using a Flow Cytometry.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 27
Illegal NheI site found at 50 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]