Difference between revisions of "Part:BBa K1554000:Design"

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===Source===
 
===Source===
  
−
Amplified from genomic DNA of Nicotiana tabacco.
+
Amplified by PCR from genomic DNA of Nicotiana tabacco.
  
 
===References===
 
===References===

Revision as of 11:27, 28 September 2014


TA29 promoter


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

BioBrick compatible


Source

Amplified by PCR from genomic DNA of Nicotiana tabacco.

References

[1] Cho HJ, Kim S, Kim M, Kim BD (2001) Production of transgenic male sterile tobacco plants with the cDNA encoding a ribosome inactivating protein in Dianthus sinensis L. Mol Cells 11:326–333

[2] Sa G, Mi M, He-Chun Y, Guo-Feng L (2002) Anther-specific expression of ipt gene in transgenic tobacco and its effect on plant development. Transgenic Res 11:269–278

[3] Shaya F, Gaiduk S, Keren I, Shevtsov S, Zemah H, Belausov E, Evenor D, Reuveni M, Ostersetzer-Biran O (2012) Expression of mitochondrial gene fragments within the tapetum induce male sterility by limiting the biogenesis of the respiratory machinery in transgenic tobacco. J Integr Plant Biol 54:115–130

[4] Kriete, G., Niehaus, K., Perlick, A. M., Puhler, A., & Broer, I. (1996) Male sterility in transgenic tobacco plants induced by tapetum-specific deacetylation of the externally applied non-toxic compounds N-acetyl- L -phosphinothricin. The Plant Journal, 9, 809–818.