Difference between revisions of "Part:BBa K1362400:Design"

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===References===
 
===References===
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[1] Joachim Zettler, Vivien Schütz, Henning D. Mootz, The naturally split Npu DnaE intein exhibits an extraordinarily high rate in the protein trans-splicing reaction, FEBS Letters, Volume 583, Issue 5, 4 March 2009, Pages 909-914, ISSN 0014-5793, http://dx.doi.org/10.1016/j.febslet.2009.02.003.

Revision as of 17:28, 6 October 2014


NpuDnaE N-Intein cloning piece


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

This part represents only the intein sequence without including the standard splicing-site or polyglycine-linker overhangs.

Source

Obtained by PCR amplification from pVS41 by Prof. Henning D. Mootz, University of Muenster.[1]

References

[1] Joachim Zettler, Vivien Schütz, Henning D. Mootz, The naturally split Npu DnaE intein exhibits an extraordinarily high rate in the protein trans-splicing reaction, FEBS Letters, Volume 583, Issue 5, 4 March 2009, Pages 909-914, ISSN 0014-5793, http://dx.doi.org/10.1016/j.febslet.2009.02.003.