Difference between revisions of "Part:BBa K1045002:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This part was amplified from ''Bacillus subtilis'' genomic DNA and ligated into the ''EcoRI'' and ''PstI'' digested pSB1C3 backbone (see part BBa_K1045004). It was then further ''SpeI'' and ''EcoRI'' digested and ligated with the ''Xba'' and ''EcoRI'' digested CFP (BBa-E0020). | + | This part was amplified from ''Bacillus subtilis'' genomic DNA and ligated into the ''EcoRI'' and ''PstI'' digested pSB1C3 backbone (see part BBa_K1045004). It was then further ''SpeI'' and ''EcoRI'' digested and ligated with the ''Xba'' and ''EcoRI'' digested CFP (BBa-E0020). Altogether this composes part BBa_K1045002. |
===Source=== | ===Source=== |
Revision as of 12:44, 25 September 2013
CFP Reporter under control of the c-di-AMP-dependent YdaO Riboswitch
Assembly Compatibility:
- 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
This part was amplified from Bacillus subtilis genomic DNA and ligated into the EcoRI and PstI digested pSB1C3 backbone (see part BBa_K1045004). It was then further SpeI and EcoRI digested and ligated with the Xba and EcoRI digested CFP (BBa-E0020). Altogether this composes part BBa_K1045002.
Source
References
Peter Y Watson & Martha J Fedor (2012) “The ydaO motif is an c-di-AMP-sensing riboswitch in Bacillus subtilis“, Nature Chemical Biology No. 8, pp. 963-965