Difference between revisions of "Part:BBa K1992009"
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__NOTOC__
 
__NOTOC__
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<partinfo>BBa_K1992008 short</partinfo>
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<partinfo>BBa_K1992009 short</partinfo>
  
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K1992008 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K1992009 SequenceAndFeatures</partinfo>
  
 
==Introduction==
 
==Introduction==

Revision as of 22:57, 21 October 2016


Tar GFP tagged expression system (promoter+RBS+coding+terminator)

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1343
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 2385
    Illegal SapI.rc site found at 172

Introduction

A GFP gene was fused to the improved expression system of the Tar chemoreceptor(BBa_K1992006). The plasmid is comprised of a promoter, a strong RBS, Tar gene, a GFP gene and a terminator. In order to obtain the fusion, a proper linker sequence was introduced between the Tar and the GFP gene.

Usage and Biology

This device was used as a proof of concept in order to verify the migration of the chemoreceptor to the poles of the bacterial membrane.

Experiments and results

Expariments and results of this exprassion system can be seen in the Tar-GFP part (BBa_K1992003) and in our result page [http://2016.igem.org/Team:Technion_Israel/Tar_improvements Tar improvements and characterzation]