Difference between revisions of "Part:BBa K2692000:Design"

 
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===Design Notes===
 
===Design Notes===
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The his tag has the ability to also bind to metals (this is why is is able to bind to a nickle column). To gain accurate results, the his tag would have to be removed to ensure that the cutA protein is binding the copper.  
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The hexahistidine tag has the ability to also bind to metals (this is why is is able to bind to a nickle column). To gain accurate results, the his tag would have to be removed to ensure that the cutA protein is binding the copper. The coding sequence is codon optimized for efficient expression in <i> E.coli <i/>
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===Source===
 
===Source===

Revision as of 03:13, 11 October 2018


CutA metal binding protein from E.coli


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

The hexahistidine tag has the ability to also bind to metals (this is why is is able to bind to a nickle column). To gain accurate results, the his tag would have to be removed to ensure that the cutA protein is binding the copper. The coding sequence is codon optimized for efficient expression in E.coli <i/>

Source

The part in plasmid was a gift from the Weiden lab at the University of Lethbridge and was a part of the ASKA database.

===References===