Difference between revisions of "Part:BBa K1789018:Design"
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<partinfo>BBa_K1789018 short</partinfo> | <partinfo>BBa_K1789018 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
− | + | 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. | + | By integrating the coding sequences of the TALE-fused proteins and the scaffold, three different plasmids can be constructed and this is the first one. |
− | [[File:GFP | + | |
− | This prototype is designed to test if our system can achieve our goal of compartmentation by examining if the green florescent intensity raised observably. | + | |
+ | [[File:Design GFP 1.jpg]] | ||
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+ | Fig. 1 Plasmid of Split GFP fused with TALE1/TALE3 on SCAF1 | ||
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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. | ||
+ | |||
Fluoroskan Ascent FL by Thermo can be used to detect the fluorescence intensity. | Fluoroskan Ascent FL by Thermo can be used to detect the fluorescence intensity. | ||
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We obtained it through the contribution of our basic subparts. | We obtained it through the contribution of our basic subparts. | ||
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Latest revision as of 10:17, 18 September 2015
GFP_S1
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2311
Illegal BamHI site found at 4908 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE 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 - 1000INCOMPATIBLE 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 first one.
Fig. 1 Plasmid of Split GFP fused with TALE1/TALE3 on SCAF1
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.