Difference between revisions of "Part:BBa K3257114"
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<partinfo>BBa_K3257114 short</partinfo> | <partinfo>BBa_K3257114 short</partinfo> | ||
− | This part includes the gene | + | This part includes the target gene, which is ChlR_E97X (https://parts.igem.org/Part:BBa_K3257037) in this part, and a set of necessary regulatory factor for the reverse transcription and recombination, such as the primer binding site (PBS https://parts.igem.org/Part:BBa_K3257063), the R region (https://parts.igem.org/Part:BBa_K3257061), the U5 region (https://parts.igem.org/Part:BBa_K3257062), the polypurine tract (PPT https://parts.igem.org/Part:BBa_K3257060) and lox sites (https://parts.igem.org/Part:BBa_K3257064 https://parts.igem.org/Part:BBa_K3257075). Together they function as a target of the reverse transcription and recombination process, making them vital and fundamental for our R-Evolution system. |
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− | <span class='h3bb'>Sequence and Features</span> | + | <span class='h3bb'>'''Sequence and Features'''</span> |
<partinfo>BBa_K3257114 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3257114 SequenceAndFeatures</partinfo> | ||
Latest revision as of 20:03, 21 October 2019
T7 Promoter-lox5171-R-PPT-RBS-ChlR_E97X-PBS-U5-R-loxP-T7 Terminator
This part includes the target gene, which is ChlR_E97X (https://parts.igem.org/Part:BBa_K3257037) in this part, and a set of necessary regulatory factor for the reverse transcription and recombination, such as the primer binding site (PBS https://parts.igem.org/Part:BBa_K3257063), the R region (https://parts.igem.org/Part:BBa_K3257061), the U5 region (https://parts.igem.org/Part:BBa_K3257062), the polypurine tract (PPT https://parts.igem.org/Part:BBa_K3257060) and lox sites (https://parts.igem.org/Part:BBa_K3257064 https://parts.igem.org/Part:BBa_K3257075). Together they function as a target of the reverse transcription and recombination process, making them vital and fundamental for our R-Evolution system.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1107
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 945
Illegal BsaI.rc site found at 966