Difference between revisions of "Part:BBa K3037003"
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<partinfo>BBa_K3037003 short</partinfo> | <partinfo>BBa_K3037003 short</partinfo> | ||
+ | {| style="color:black" cellpadding="6" cellspacing="1" border="2" align="right" | ||
+ | ! colspan="2" style="background:#FFBF00;"|Fusion protein | ||
+ | |- | ||
+ | |'''Function''' | ||
+ | |Colour detection of specific DNA sequences | ||
+ | |- | ||
+ | |'''Use in''' | ||
+ | |<span style="font-style: italic;">Escherichia coli</span> | ||
+ | |- | ||
+ | |'''RFC standard''' | ||
+ | |RFC 25 compatible | ||
+ | |- | ||
+ | |'''Backbone''' | ||
+ | |pSB1C3<br> | ||
+ | |- | ||
+ | |'''Submitted by''' | ||
+ | |Team:TU_Dresden 2019[https://2019.igem.org/Team:TU_Dresden] | ||
+ | |} | ||
+ | |||
+ | |||
+ | === Overview === | ||
The TU Dresden 2019 team design this biobrick in order to create a system for the short and quick detection of specific DNA sequences. | The TU Dresden 2019 team design this biobrick in order to create a system for the short and quick detection of specific DNA sequences. | ||
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+ | === Sequence === | ||
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<partinfo>BBa_K3037003 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3037003 SequenceAndFeatures</partinfo> | ||
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Revision as of 23:49, 14 October 2019
Fusion protein dCas9 + HRP (MBP/dCas9/linker/HRP/Strep-tag)
Fusion protein | |
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Function | Colour detection of specific DNA sequences |
Use in | Escherichia coli |
RFC standard | RFC 25 compatible |
Backbone | pSB1C3 |
Submitted by | Team:TU_Dresden 2019[1] |
Overview
The TU Dresden 2019 team design this biobrick in order to create a system for the short and quick detection of specific DNA sequences.
The plasmid used for the expression of the construct was pSB1C3.
Sequence
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 2302
Illegal NheI site found at 5500 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 381
Illegal BglII site found at 5742
Illegal BamHI site found at 4581
Illegal BamHI site found at 5314
Illegal XhoI site found at 5826 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 79