Difference between revisions of "Part:BBa K4361302"

 
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<partinfo>BBa_K4361302 short</partinfo>
 
<partinfo>BBa_K4361302 short</partinfo>
  
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A mutant of the BlcR protein, created through site-directed mutagenesis with primers R4 ([[Part:BBa_K4361204]]) and F4.1 D37V ([[Part:BBa_K4361205]]). For this mutant, the alanine in position 40 has been changed to valine by mutating the GCG codon to GTG.
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A mutant of the BlcR protein, created through site-directed mutagenesis with primers R4 ([[Part:BBa_K4361204]]) and F4.1 A40V ([[Part:BBa_K4361205]]). For this mutant, the alanine in position 40 has been changed to valine by mutating the GCG codon to GTG.
  
 
This mutant also contains the following nucleotide mutations outside of the targeted site:
 
This mutant also contains the following nucleotide mutations outside of the targeted site:

Revision as of 12:17, 19 September 2022


BlcR A40V

A mutant of the BlcR protein, created through site-directed mutagenesis with primers R4 (Part:BBa_K4361204) and F4.1 A40V (Part:BBa_K4361205). For this mutant, the alanine in position 40 has been changed to valine by mutating the GCG codon to GTG.

This mutant also contains the following nucleotide mutations outside of the targeted site:

  • .

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 694
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 78
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 589