Difference between revisions of "Part:BBa K2130012"
 
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<partinfo>BBa_K2130012 short</partinfo>
  
 
dCas9 is a catalytically inactive Cas9, which still retains it's ability to bind to DNA. For epigenetic regulation, the dCas9 is highly dependent upon the function of it's fusion partner.  
 
dCas9 is a catalytically inactive Cas9, which still retains it's ability to bind to DNA. For epigenetic regulation, the dCas9 is highly dependent upon the function of it's fusion partner.  
  
 
For this part, we have deleted the HNH domain of the SP-dCas9 and tested it's binding capability by assessing the strength in transcriptional activation via a VP64-p65-Rta.
 
For this part, we have deleted the HNH domain of the SP-dCas9 and tested it's binding capability by assessing the strength in transcriptional activation via a VP64-p65-Rta.
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https://static.igem.org/mediawiki/2016/8/8c/T--NTU-Singapore--NUC.png
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<p style="font-size:18px; text-align: center;">Activation of ZsGreen reporter gene using NUC and REC truncations</p>
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K2130000 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K2130012 SequenceAndFeatures</partinfo>
  
  
 
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===Functional Parameters===
 
===Functional Parameters===
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<partinfo>BBa_K2130000 parameters</partinfo>
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<partinfo>BBa_K2130012 parameters</partinfo>
 
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Latest revision as of 07:49, 19 October 2016


∆HNH Sp-dCas9

dCas9 is a catalytically inactive Cas9, which still retains it's ability to bind to DNA. For epigenetic regulation, the dCas9 is highly dependent upon the function of it's fusion partner.

For this part, we have deleted the HNH domain of the SP-dCas9 and tested it's binding capability by assessing the strength in transcriptional activation via a VP64-p65-Rta.

T--NTU-Singapore--NUC.png



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 251
    Illegal BglII site found at 1188
    Illegal BamHI site found at 2006
    Illegal XhoI site found at 3154
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 2350
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 2496
    Illegal BsaI site found at 3350
    Illegal BsaI.rc site found at 1411