Difference between revisions of "Part:BBa K4361318"

 
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A mutant of the BlcR protein, created through site-directed mutagenesis with primers R3 ([[Part:BBa_K4361218]]) and F3.9 V68S ([[Part:BBa_K4361227]]). For this mutant, the valine in position 68 has been changed to serine by mutating the GTG codon to AGC.
 
A mutant of the BlcR protein, created through site-directed mutagenesis with primers R3 ([[Part:BBa_K4361218]]) and F3.9 V68S ([[Part:BBa_K4361227]]). For this mutant, the valine in position 68 has been changed to serine by mutating the GTG codon to AGC.
  
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This mutant also contains the following nucleotide mutations outside of the targeted site:
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This mutant contains no nucleotide substitutions or indels outside of the targeted site.
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<ul>
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<li>.</li>
 
<li>.</li>

Revision as of 14:38, 22 September 2022


BlcR V68S

A mutant of the BlcR protein, created through site-directed mutagenesis with primers R3 (Part:BBa_K4361218) and F3.9 V68S (Part:BBa_K4361227). For this mutant, the valine in position 68 has been changed to serine by mutating the GTG codon to AGC.

This mutant contains no nucleotide substitutions or indels outside of the targeted site.

  • .

    • </ul>

    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