Difference between revisions of "Part:BBa K945002"
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K945002 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K945002 SequenceAndFeatures</partinfo>
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===Part Contributions===
 +
Team Washington 2016 has removed RFC[10] illegal restriction sites from this part as an improvement to its functionality so that it may be used in other biobricks.  The part can be found here: https://parts.igem.org/Part:BBa_K2165004 as part K2165004, along with further documentation and data on it.
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===Promoter characterization===
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Team Czech Republic 2015 used this promoter very extensively. As a result, the characterization of this part was improved. See the [[Part:BBa_K945002:Experience|Experience page]] for details.
  
 
===Promoter Strength===
 
===Promoter Strength===
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Tec-Monterrey Ekam is working on further characterizing the functionality of this part through the use of GFP as a reporter gene, which will be finalized shortly.
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Tec-Monterrey Ekam is working on '''quantitatively''' characterizing the functionality of this part through the use of <partinfo>BBa_K945004</partinfo> (GFP) as a reporter, which will be finalized shortly.
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  

Latest revision as of 06:14, 19 October 2016

CUP1 yeast promoter

This sequence contains the inducible transcription promoter CUP1, useful for controlled gene expression which is actively enhanced in yeasts in the presence of copper.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 279
    Illegal XbaI site found at 517
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal PstI site found at 49
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal PstI site found at 49
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 55
    Illegal BamHI site found at 510
    Illegal XhoI site found at 8
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 279
    Illegal XbaI site found at 517
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal PstI site found at 49
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 279
    Illegal XbaI site found at 517
    Illegal SpeI site found at 343
    Illegal SpeI site found at 523
    Illegal PstI site found at 49
    Illegal NgoMIV site found at 36
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 529

Part Contributions

Team Washington 2016 has removed RFC[10] illegal restriction sites from this part as an improvement to its functionality so that it may be used in other biobricks. The part can be found here: https://parts.igem.org/Part:BBa_K2165004 as part K2165004, along with further documentation and data on it.

Promoter characterization

Team Czech Republic 2015 used this promoter very extensively. As a result, the characterization of this part was improved. See the Experience page for details.

Promoter Strength

Tec-Monterrey Ekam is working on quantitatively characterizing the functionality of this part through the use of BBa_K945004 (GFP) as a reporter, which will be finalized shortly.