Difference between revisions of "Part:BBa K1321367"
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<partinfo>BBa_K1321367 short</partinfo> | <partinfo>BBa_K1321367 short</partinfo> | ||
− | + | A T7-promoter expression construct of super-folder GFP fused N-terminally to CBDcipA (a cellulose-binding domain), which contains an endogenous N and C-terminal linker sequence. | |
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+ | This construct is part of a library of Super-folder GFP fusions with cellulose binding domains, which we used to assay the CBD binding affinity. Please see our [http://2014.igem.org/Team:Imperial/Functionalisation project page] for more information. The collection of sfGFP-CBD fusion parts can be seen in the table below: [[File:IC14-sfGFP-part-table.PNG]] | ||
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+ | Note that the stop codon plus 6 bp at the end of the sequence are included the RFC25 suffix which is not shown. The prefix to this part is RFC10 format. | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 18:33, 17 October 2014
sfGFP + linker-CBDcipA-linker with T7 promoter
A T7-promoter expression construct of super-folder GFP fused N-terminally to CBDcipA (a cellulose-binding domain), which contains an endogenous N and C-terminal linker sequence.
This construct is part of a library of Super-folder GFP fusions with cellulose binding domains, which we used to assay the CBD binding affinity. Please see our [http://2014.igem.org/Team:Imperial/Functionalisation project page] for more information. The collection of sfGFP-CBD fusion parts can be seen in the table below:
Note that the stop codon plus 6 bp at the end of the sequence are included the RFC25 suffix which is not shown. The prefix to this part is RFC10 format.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 923
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 923
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 923
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 923
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 923
Illegal NgoMIV site found at 53 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 68