Difference between revisions of "Part:BBa K1680020"
 
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<partinfo>BBa_K1680020 short</partinfo>
 
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Protein coding region for a fusion construct of Cre Recombinase (BBa_K1680007) and 145N Dronpa (BBa_K1680006) with intermediate 15 amino acid linker (BBa_K1680003). Oligomerisation of Dronpa (Tetramer) should stop Cre from accessing DNA in the nucleus thereby inhibiting it until light deactivation of Dronpa by illuminating with 488nm light. Dronpa can be reactivated by illumination with 405nm light. Part is cloned in the pTUM104 (BBa_K801004) and thereby galactose inducible.
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Protein coding region for a fusion construct of Cre Recombinase ([[Part:BBa_K1680007]]) and 145N Dronpa ([[Part:BBa_K1680006]]) with intermediate 15 amino acid linker ([[Part:BBa_K1680003]]). Oligomerisation of Dronpa (Tetramer) should stop Cre from accessing DNA in the nucleus thereby inhibiting it until light deactivation of Dronpa by illuminating with 488nm light. Dronpa can be reactivated by illumination with 405nm light.
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This Part is cloned and shipped in the pTUM104 ([[Part:BBa_K801004]]) and thereby galactose inducible in yeast.
  
 
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<span class='h3bb'>Sequence and Features</span>
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<span class='h3bb'>'''Sequence and Features'''</span>
 
<partinfo>BBa_K1680020 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K1680020 SequenceAndFeatures</partinfo>
  

Latest revision as of 02:20, 26 September 2015

Cre-dronpa fusion

Protein coding region for a fusion construct of Cre Recombinase (Part:BBa_K1680007) and 145N Dronpa (Part:BBa_K1680006) with intermediate 15 amino acid linker (Part:BBa_K1680003). Oligomerisation of Dronpa (Tetramer) should stop Cre from accessing DNA in the nucleus thereby inhibiting it until light deactivation of Dronpa by illuminating with 488nm light. Dronpa can be reactivated by illumination with 405nm light.

This Part is cloned and shipped in the pTUM104 (Part:BBa_K801004) and thereby galactose inducible in yeast.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1381
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 476