Difference between revisions of "Part:BBa K2520006"

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<span class='h3bb'>Sequence and Features</span>
 
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<partinfo>BBa_K2520006 SequenceAndFeatures</partinfo>
 
  
  
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In this device, the inducible protein is GFP, and can be used easily for calibration and characterization of inducible systems. The human growth hormone (hGH) terminator has been added to allow for efficient expression of the GFP.  
 
In this device, the inducible protein is GFP, and can be used easily for calibration and characterization of inducible systems. The human growth hormone (hGH) terminator has been added to allow for efficient expression of the GFP.  
  
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<partinfo>BBa_K2520006 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2520006 parameters</partinfo>
 
<partinfo>BBa_K2520006 parameters</partinfo>
 
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Revision as of 07:17, 27 October 2017

TRE-GFP-hGH

This device allows inducible expression of GFP within mammalian cells. The TRE promoter is made up of Tet operator (TetO) sequence concatemers fused to a minimal hCMV. This promoter can be used for inducible expression of the downstream gene in two different schemes.

Tet-off

In the absence of Dox, tTA binds to the TRE promoter and activates transcription of the downstream gene. In the presence of Dox, tTA cannot bind to the TRE, and expression from the target gene remains minimal. Sequence and Features


Tet-on

In the presence of Dox, rtTA binds the TRE promoter and activates transcription of the downstream gene. In the absence of Dox, rtTA cannot bind the TRE promoter, and expression of the downstream gene is minimal.

Usage and Biology

In this device, the inducible protein is GFP, and can be used easily for calibration and characterization of inducible systems. The human growth hormone (hGH) terminator has been added to allow for efficient expression of the GFP.


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1438
    Illegal BsaI.rc site found at 967