Difference between revisions of "Part:BBa K2340002:Design"

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===References===
 
===References===
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East-Selesky, A. <i>et al.</i> (2016) Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection. <i>Nature</i> <b>538:</b> 270–273.

Revision as of 17:02, 31 October 2017


Guide RNA construct of human ꞵ-actin (2)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 217
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 183
    Illegal XhoI site found at 224
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The sequence complementary tot the human ꞵ-actin had to be exclusively complementary to that. If complementary to other mRNA sequences, the Cas13 could target those as well


Source

Sequences for crRNA backbone were taken from East-Selesky et al (2016).


The complementary sequence to human ꞵ-actin mRNA and the sequences of the human U6 promoter and terminator are taken from Genbank

References

East-Selesky, A. et al. (2016) Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection. Nature 538: 270–273.