Difference between revisions of "Part:BBa K4361000"

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Firstly, the wildtype sequence was scrambled using the Genscript Sequence Scramble tool (https://www.genscript.com/tools/create-scrambled-sequence) to create an oligo containing the same nucleotides in a randomized order. Since this oligo does not contain either of the inverted repeat pairs, BlcR should not be able to specifically bind this molecule, thus it can be used as a negative control to compare other sequences to. This oligo was designated BBa_K4361000.
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Shares nucleotides of BBa_K4361001, but in a scrambled order as to no longer allow specific binding.
 
Shares nucleotides of BBa_K4361001, but in a scrambled order as to no longer allow specific binding.
  
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===Usage and Biology===
 
===Usage and Biology===
  

Revision as of 13:51, 6 October 2022


BlcR-binding oligo, 51 bp, scrambled


Firstly, the wildtype sequence was scrambled using the Genscript Sequence Scramble tool (https://www.genscript.com/tools/create-scrambled-sequence) to create an oligo containing the same nucleotides in a randomized order. Since this oligo does not contain either of the inverted repeat pairs, BlcR should not be able to specifically bind this molecule, thus it can be used as a negative control to compare other sequences to. This oligo was designated BBa_K4361000.


Shares nucleotides of BBa_K4361001, but in a scrambled order as to no longer allow specific binding.

Usage and Biology

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 37
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 37
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 37
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal SpeI site found at 37
  • 1000
    COMPATIBLE WITH RFC[1000]