Difference between revisions of "Part:BBa K1968001:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | Nucleotide | + | Nucleotide G at position 109 was mutated to a A in order to remove a BbsI site, which would have interfered with later MoClo assemblies. |
Revision as of 19:01, 9 October 2016
Synechocystis Pcpc560 Phytobrick promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2
Design Notes
Nucleotide G at position 109 was mutated to a A in order to remove a BbsI site, which would have interfered with later MoClo assemblies.
Source
The part was ordered as gblock through IDT and was subsequently cloned into PhytoBricks Universal Acceptor plasmids (BBa_P10500).