Difference between revisions of "Part:BBa K3286041"

 
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By doing so, we can generate very fast, cheap and reliable a library of CRISPR arrays*.
 
By doing so, we can generate very fast, cheap and reliable a library of CRISPR arrays*.
  
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* We have observed that insertion of two spacers (with a repeat in the middle) is also possible with the use of ultramers.
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    *We have observed that insertion of two spacers (with a repeat in the middle) is also possible with the use of ultramers.
  
  

Revision as of 13:43, 14 October 2019


F. novicida Cpf1 (Cas12a) CRISPR array

Francisella novicida Cpf1 (Cas12a) CRISPR array .

The Cpf1 (Cas12a) CRISPR array of F. novicida, with two repeats and a scrambled (non-targeting) spacer.

New spacers can be generated by BbsI digestion of the CRISPR array and ligation of two annealed oligo's (with 5'-AGAT... and 5'-AGAC overhangs). By doing so, we can generate very fast, cheap and reliable a library of CRISPR arrays*. 

   *We have observed that insertion of two spacers (with a repeat in the middle) is also possible with the use of ultramers.


Sequence and Features


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
    COMPATIBLE WITH RFC[1000]