Difference between revisions of "Part:BBa K1789019:Design"

 
 
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<partinfo>BBa_K1789019 short</partinfo>
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<partinfo>BBa_K1789018 short</partinfo>
  
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<partinfo>BBa_K1789019 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K1789018 SequenceAndFeatures</partinfo>
  
  
 
===Design Notes===
 
===Design Notes===
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This is the first experimental group of our project. Our theory is feasible if the functional parameter of this group is stronger than the group of negative control.
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In our project, we demonstrated a prototype by fusing the Amino (or Carboxyl) Half of GFP with TALE1 (or TALE2/3).  
  
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By integrating the coding sequences of the TALE-fused proteins and the scaffold, three different plasmids can be constructed and this is the second one.
  
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[[File:Design GFP 2.jpg]]
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Fig. 1 Plasmid of Split GFP fused with TALE1/TALE2 on SCAF2
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This prototype is designed to test if our system can achieve our goal of compartmentation by examining if the green florescent intensity raised observably.
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Fluoroskan Ascent FL by Thermo can be used to detect the fluorescence intensity.
  
 
===Source===
 
===Source===
  
 
We obtained it through the contribution of our basic subparts.
 
We obtained it through the contribution of our basic subparts.
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===References===
 

Latest revision as of 12:52, 18 September 2015

GFP_S1


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 2311
    Illegal BamHI site found at 4908
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 5323
    Illegal AgeI site found at 5353
    Illegal AgeI site found at 5383
    Illegal AgeI site found at 5413
    Illegal AgeI site found at 5443
    Illegal AgeI site found at 5473
    Illegal AgeI site found at 5503
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1304
    Illegal BsaI.rc site found at 3390
    Illegal BsaI.rc site found at 3798
    Illegal BsaI.rc site found at 4104
    Illegal BsaI.rc site found at 5094


Design Notes

In our project, we demonstrated a prototype by fusing the Amino (or Carboxyl) Half of GFP with TALE1 (or TALE2/3).

By integrating the coding sequences of the TALE-fused proteins and the scaffold, three different plasmids can be constructed and this is the second one.


Design GFP 2.jpg

Fig. 1 Plasmid of Split GFP fused with TALE1/TALE2 on SCAF2


This prototype is designed to test if our system can achieve our goal of compartmentation by examining if the green florescent intensity raised observably.

Fluoroskan Ascent FL by Thermo can be used to detect the fluorescence intensity.

Source

We obtained it through the contribution of our basic subparts.