Difference between revisions of "Part:BBa K537007:Design"

 
(Design Notes)
 
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__NOTOC__
 
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<partinfo>BBa_K537007 short</partinfo>
 
<partinfo>BBa_K537007 short</partinfo>
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===Design Notes===
 
===Design Notes===
None
 
  
 +
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 primers
+
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:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE 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.

References