Difference between revisions of "Part:BBa K1475003:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | The part was constructed by | + | The part was constructed by removing the LVA rapid [https://parts.igem.org/Protein_domains/Degradation degradation tag] from the iGEM registry part TetR+LVA ([https://parts.igem.org/Part:BBa_K1475003 Part:BBa_C0040]) using the following primers. |
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Forward primer: | Forward primer: | ||
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TTTCTGCAGCGGCCGCTACTAGTATTATTAGGACCCACTTTCACATTTAAGTTGTTTTTC | TTTCTGCAGCGGCCGCTACTAGTATTATTAGGACCCACTTTCACATTTAAGTTGTTTTTC | ||
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===Source=== | ===Source=== |
Revision as of 20:33, 15 October 2014
tetracyclin repressor from transposon Tn10
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The part was constructed by removing the LVA rapid degradation tag from the iGEM registry part TetR+LVA (Part:BBa_C0040) using the following primers.
Forward primer:
AAGAATTCGCGGCCGCTTCTAGATGTCCAGATTAGATAAAAGTAAAGTGATTAACAGCG
Reverse primer:
TTTCTGCAGCGGCCGCTACTAGTATTATTAGGACCCACTTTCACATTTAAGTTGTTTTTC
Source
Organizm: Escherichia coli
References
1. Tetsystems, 2008: Principles and Components Description. http://www.tetsystems.com/science-technology/principles-components
2. C. Krafft, et al.: Interaction of Tet Repressor with Operator DNA and with Tetracycline Studied by Infrared and Raman Spectroscopy. Biophysical Journal, Volume 74, Issue 1, January 1998, Pages 63–71. http://www.sciencedirect.com/science/article/pii/S0006349598777677