Difference between revisions of "Part:BBa K3037003"

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__NOTOC__
 
 
<partinfo>BBa_K3037003 short</partinfo>
 
<partinfo>BBa_K3037003 short</partinfo>
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{| style="color:black" cellpadding="6" cellspacing="1" border="2" align="right"
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! colspan="2" style="background:#FFBF00;"|Fusion protein
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|-
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|'''Function'''
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|Colour detection of specific DNA sequences
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|-
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|'''Use in'''
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|<span style="font-style: italic;">Escherichia coli</span>
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|-
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|'''RFC standard'''
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|RFC 25 compatible
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|-
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|'''Backbone'''
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|pSB1C3<br>
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|-
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|'''Submitted by'''
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|Team:TU_Dresden 2019[https://2019.igem.org/Team:TU_Dresden]
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|}
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=== 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 ===
  
<!-- Add more about the biology of this part here
 
===Usage and Biology===
 
 
<!-- -->
 
<span class='h3bb'>Sequence and Features</span>
 
 
<partinfo>BBa_K3037003 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K3037003 SequenceAndFeatures</partinfo>
 
 
<!-- Uncomment this to enable Functional Parameter display
 
===Functional Parameters===
 
<partinfo>BBa_K3037003 parameters</partinfo>
 
<!-- -->
 

Revision as of 23:49, 14 October 2019

Fusion protein dCas9 + HRP (MBP/dCas9/linker/HRP/Strep-tag)

Fusion protein
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:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 2302
    Illegal NheI site found at 5500
  • 21
    INCOMPATIBLE 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
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 79