Difference between revisions of "Part:BBa K784030"
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<partinfo>BBa_K784030 short</partinfo> | <partinfo>BBa_K784030 short</partinfo> | ||
− | This part consists of | + | This part consists of SP6 RNA polymerase induced promoter followed by an RBS and the ‎Alkaline Phosphatase reporter gene (pHOA) from Citrobacter.‎ |
− | The part's purpose is to monitor the translation of the | + | The part's purpose is to monitor the translation of the SP6 RNA polymerase with the Alkaline ‎Phosphatase gene which can be quantified with the [https://parts.igem.org/Arkin_JCA_PNPAssay PNP (para-nitrophenol phosphate) hydrolysis assay] that has been ‎made by Arkin Lab group in 2006.‎ |
The Alkaline Phosphatase + RBS part is between XmaI and XhoI restriction sites and ‎therefore can be excised out by these enzymes. | The Alkaline Phosphatase + RBS part is between XmaI and XhoI restriction sites and ‎therefore can be excised out by these enzymes. | ||
Latest revision as of 21:48, 18 September 2012
pSP6+RBS+Alkaline Phosphatase (pHO)+Terminator
This part consists of SP6 RNA polymerase induced promoter followed by an RBS and the Alkaline Phosphatase reporter gene (pHOA) from Citrobacter. The part's purpose is to monitor the translation of the SP6 RNA polymerase with the Alkaline Phosphatase gene which can be quantified with the PNP (para-nitrophenol phosphate) hydrolysis assay that has been made by Arkin Lab group in 2006. The Alkaline Phosphatase + RBS part is between XmaI and XhoI restriction sites and therefore can be excised out by these enzymes.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1506
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1506
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1506
Illegal XhoI site found at 18 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1506
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1506
Illegal NgoMIV site found at 345
Illegal NgoMIV site found at 792 - 1000COMPATIBLE WITH RFC[1000]