Difference between revisions of "Part:BBa K2560118:Design"

 
 
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===Design Notes===
 
===Design Notes===
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More informations coming soon!
 
  
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The sequence was obtained from part <a href="https://parts.igem.org/Part:BBa_M0050">BBa_M0050</a>. The parts sequence was not changed apart from adding the promoter overhangs that are required for subsequent cloning.
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===Source===
 
===Source===
  
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More informations coming soon!
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<html>
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The part was created by annealing single stranded oligonucleotides and subsequent integration into the part entry vector <a href="https://parts.igem.org/Part:BBa_K2560002">BBa_K2560002</a> using Golden Gate assembly. If you stuggle with <i> de novo </i> synthesis we recomended this
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<a href="https://parts.igem.org/Help:Promoters/Construction">site</a>.
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<b> Forward Oligo:</b>
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CTCGGCTTTAGCTGCTAACGACGAAAACTACGCTCTGGCTGCTTAGGGGTA
  
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===References===
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<b> Reverse Oligo:</b>
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CCTCATACCCCTAAGCAGCCAGAGCGTAGTTTTCGTCGTTAGCAGCTAAAGC

Latest revision as of 01:06, 18 October 2018


Phytobrick version of 5a BBa_M0050 SsrA degradation tag


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]


Design Notes

The sequence was obtained from part BBa_M0050. The parts sequence was not changed apart from adding the promoter overhangs that are required for subsequent cloning.

Source

The part was created by annealing single stranded oligonucleotides and subsequent integration into the part entry vector BBa_K2560002 using Golden Gate assembly. If you stuggle with de novo synthesis we recomended this site.

Forward Oligo: CTCGGCTTTAGCTGCTAACGACGAAAACTACGCTCTGGCTGCTTAGGGGTA

Reverse Oligo: CCTCATACCCCTAAGCAGCCAGAGCGTAGTTTTCGTCGTTAGCAGCTAAAGC