Difference between revisions of "Part:BBa K537007:Design"
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===Design Notes=== | ===Design Notes=== | ||
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+ | This biobrick part represents a composite of a RBS directly upstream of an E.coli CheZ motility factor. | ||
+ | This part represents an N-terminal fusion part. The part contains a standard prefix and a “assembly standard 25” suffix (Freiburg Fusions/ RFC 25). Because of multiple AgeI sites within CheZ, full compatibility with RFC 25 could is not maintained. Cloning to a C-terminal part occurs by cutting with NgoMI. The CheZ CDS therefore lacks a TAATAA double stop codon (TAG stop provided by RFC 25 suffix). | ||
===Source=== | ===Source=== | ||
− | PCR | + | The CheZ sequence was PCR amplified from E.coli strain DH5α. |
===References=== | ===References=== |
Latest revision as of 13:46, 18 September 2011
RBS CheZ N-Fusion
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This biobrick part represents a composite of a RBS directly upstream of an E.coli CheZ motility factor.
This part represents an N-terminal fusion part. The part contains a standard prefix and a “assembly standard 25” suffix (Freiburg Fusions/ RFC 25). Because of multiple AgeI sites within CheZ, full compatibility with RFC 25 could is not maintained. Cloning to a C-terminal part occurs by cutting with NgoMI. The CheZ CDS therefore lacks a TAATAA double stop codon (TAG stop provided by RFC 25 suffix).
Source
The CheZ sequence was PCR amplified from E.coli strain DH5α.