Difference between revisions of "Part:BBa K1699001:Design"

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===Design Notes===
 
===Design Notes===
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Cloned into pSB1C3 using EcoRI and PstI restrictoion sites.
  
 
===Source===
 
===Source===

Revision as of 19:02, 5 September 2015

Human short TERT 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

Cloned into pSB1C3 using EcoRI and PstI restrictoion sites.

Source

DNA Synthesis by Synthezza Bioscience. Cloning into iGEM vector was done by iGEM BGU 2015.

References

1. The telomerase reverse transcriptase promoter drives efficacious tumor suicide gene therapy while preventing hepatotoxicity encountered with constitutive promoters http://www.nature.com/gt/journal/v8/n7/pdf/3301421a.pdf