Difference between revisions of "Part:BBa K1694037"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1694037 short</partinfo> | <partinfo>BBa_K1694037 short</partinfo> | ||
− | The | + | <h1>'''Introduction'''</h1> |
+ | The transmembrane protein, FadL, fused with the GBP, can act as an anchoring motif for displaying GBP on the surface of E.coli. To achieve the convenient observation, the genetic sequence of green fluorescent protein was introduced in our design. With the dual display of the GBP and the GFP, the E.coli can not only bind on the gold surface but also produce green fluorescent signal. | ||
+ | |||
+ | <h2>'''Experiment'''</h2> | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 10:06, 20 September 2015
Pcons+B0034+FadL-GBP+B0030+GFP+J61048
Introduction
The transmembrane protein, FadL, fused with the GBP, can act as an anchoring motif for displaying GBP on the surface of E.coli. To achieve the convenient observation, the genetic sequence of green fluorescent protein was introduced in our design. With the dual display of the GBP and the GFP, the E.coli can not only bind on the gold surface but also produce green fluorescent signal.
Experiment
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 499
Illegal BamHI site found at 985 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 275
Illegal NgoMIV site found at 767
Illegal NgoMIV site found at 1192
Illegal NgoMIV site found at 2102
Illegal AgeI site found at 908 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2018