Difference between revisions of "Part:BBa K2688025"
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This corrected version is devoid of extra-sequences and is therefore convenient for a direct biobrick cloning of RBS-CDS under the control of J23108 promoter. | This corrected version is devoid of extra-sequences and is therefore convenient for a direct biobrick cloning of RBS-CDS under the control of J23108 promoter. | ||
+ | |||
+ | '''For details on the process, see [[http://2018.igem.org/Team:GO_Paris-Saclay/Improve| http://2018.igem.org/Team:GO_Paris-Saclay/Improve]]''' | ||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K2688025 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2688025 SequenceAndFeatures</partinfo> |
Revision as of 19:00, 12 October 2018
J23108_corrected
J23108 promoter is part of the Chris Anderson’s collection of plasmid. The pSB1C3-BBa_J23108 was obtained by PCR mutagenesis of the pSB1C3-BBa_J23119.
This biobrick is a corrected version of the initial biobrick (BBa_J23108) obtained from (2018 – Plate 4 – 4C) position which contains extra-sequences (notably SpeI forbidden sites).
This corrected version is devoid of extra-sequences and is therefore convenient for a direct biobrick cloning of RBS-CDS under the control of J23108 promoter.
For details on the process, see http://2018.igem.org/Team:GO_Paris-Saclay/Improve
Sequence and Features
Assembly Compatibility:
- 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]