Difference between revisions of "Part:BBa K2130009"
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For this part, we have deleted the HNH and REC2 domain of the SP-dCas9 and tested it's binding capability by assessing the strength in transcriptional activation via a VP64-p65-Rta(not included in this part).
 
For this part, we have deleted the HNH and REC2 domain of the SP-dCas9 and tested it's binding capability by assessing the strength in transcriptional activation via a VP64-p65-Rta(not included in this part).
  
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https://static.igem.org/mediawiki/2016/e/e2/T--NTU-Singapore--conclusion.png
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[[File:T--NTU-Singapore--conclusion.png|400px|thumb|left|alt text]]
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 04:41, 22 October 2016


∆HNH ∆REC2 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 and REC2 domain of the SP-dCas9 and tested it's binding capability by assessing the strength in transcriptional activation via a VP64-p65-Rta(not included in this part).

File:T--NTU-Singapore--conclusion.png
alt text


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 804
    Illegal BamHI site found at 1622
    Illegal XhoI site found at 2770
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1966
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 2112
    Illegal BsaI site found at 2966
    Illegal BsaI.rc site found at 1027