Difference between revisions of "Part:BBa K2694000:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | - | + | This circuit was designed to produce the biobrick <bbpart>BBa_K2694001</bbpart>. The IPTG inducible LacI promoter and a strong ribosome binding site. A double terminator was used at the end of the circuit to prevent continued read-through. |
− | |||
− | - | + | ===Source=== |
+ | Wilhelm et al., J Bacteriol, 1999, 6977-86 and BBa_K2694000. Synthesized through BioBasic. | ||
===References=== | ===References=== |
Revision as of 00:40, 12 October 2018
EstA generator under control of pLac promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 296
Illegal BglII site found at 443 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 226
Illegal NgoMIV site found at 682
Illegal NgoMIV site found at 820
Illegal NgoMIV site found at 1360
Illegal NgoMIV site found at 1729 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
This circuit was designed to produce the biobrick BBa_K2694001. The IPTG inducible LacI promoter and a strong ribosome binding site. A double terminator was used at the end of the circuit to prevent continued read-through.
Source
Wilhelm et al., J Bacteriol, 1999, 6977-86 and BBa_K2694000. Synthesized through BioBasic.