Difference between revisions of "Part:BBa K2560007"
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− | + | <p align="justify">This is the Phytobrick version of the promoter <a href="https://parts.igem.org/Part:BBa_J23100">BBa_J23100</a> and was build as a part of the Marburg Collection. Instructions of how to use the Marburg Collection are provided at the bottom of the page. </p> | |
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Revision as of 19:31, 11 October 2018
Phytobrick version of BBa_J23100
This is the Phytobrick version of the promoter BBa_J23100 and was build as a part of the Marburg Collection. Instructions of how to use the Marburg Collection are provided at the bottom of the page.
Variant Lux (au) K2560131 (Dummy) 0.025 K2560019 (J23103) 0.032 K2560026 (J23113) 0,038 K2560023 (J23109) 0,052 K2560009 (J23104) 0,058 K2560029 (J23117) 0,090 K2560025 (J23111) 0,098 K2560028 (J23116) 0,134 K2560021 (J23107) 0,136 K2560027 (J23114) 0,163 K2560024 (J23110) 0,169 K2560018 (J23102) 0,245 K2560030 (J23118) 0,348 K2560020 (J23105) 0,387 K2560015 (J23115) 0,398 K2560014 (J23106) 0,502 K2560017 (J23101) 0,510 K2560022 (J23108) 0,768 K2560007 (J23100) 1
Usage and Biology
This is the Phytobrick version of the promoter BBa_J23100. We build up this part via de novo synthesis by annealing the single-stranded complementary oligonucleotides aiGEM1009_J23100_fwd and aiGEM1010_J23100_rev to form the double-stranded Anderson Promotor
BBa_J23100. If you stuggle with de novo synthesis we recomended this site on the iGEM Wiki.
Marburg 2018 characterized this part in Vibrio natriegens using the lux operon of Photorhabdus luminescens (BBa_K2560051). The messured relative promotor strenghts in Vibrio natriegens were correlated to the relative promotor strenghts in E. coli (iGEM Berkeley 2006).
The parts sequence was verified by Sanger sequencing.
Sequence and Features
- 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]
Marburg Toolbox
We proudly present the Marburg Collection, a novel golden-gate-based toolbox containing various parts that are compatible with the PhytoBrick system and MoClo. Compared to other bacterial toolboxes, the Marburg Collection shines with superior flexibility. We overcame the rigid paradigm of plasmid construction - thinking in fixed backbone and insert categories - by achieving complete de novo assembly of plasmids. 36 connectors facilitate flexible cloning of multigene constructs and even allow for the inversion of individual transcription units. Additionally, our connectors function as insulators to avoid undesired crosstalk. The Marburg Collection contains 137 parts in total, including: inducible promoters, reporters, fluorescence and epitope tags, Oris, resistance cassettes and a set of project related components. To increase the value of the Marburg Collection, we additionally provide detailed experimental characterization for V. natriegens and a supportive software. We aspire availability of our toolbox for future iGEM teams to empower accelerated progression in their ambitious projects.