Difference between revisions of "Part:BBa K1694035"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1694035 short</partinfo> | <partinfo>BBa_K1694035 short</partinfo> | ||
| − | + | <h1>'''Introduction:'''</h1> | |
The engineered E.coli could express both scFv of anti-Her2 and blue flourescent. | The engineered E.coli could express both scFv of anti-Her2 and blue flourescent. | ||
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| + | To prove that our scFv can actually bind on to the antigen on cancer cells, we connected each scFv with a different fluorescence protein. Therefore we could use fluorescence microscope to clearly observe if the E. coli has produced scFv proteins. Currently, we built three different scFv connected with their respectively fluorescence protein. When applied on cell staining, we can identify the antigen distribution on cancer cells by observing the fluorescence. Furthermore, if we use the three scFv simultaneously, we can also detect multiple markers. | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
Revision as of 17:32, 18 September 2015
Pcons+B0034+Lpp-OmpA-N+scFv(Anti-HER2)+B0030+GFP+J61048
Introduction:
The engineered E.coli could express both scFv of anti-Her2 and blue flourescent.
To prove that our scFv can actually bind on to the antigen on cancer cells, we connected each scFv with a different fluorescence protein. Therefore we could use fluorescence microscope to clearly observe if the E. coli has produced scFv proteins. Currently, we built three different scFv connected with their respectively fluorescence protein. When applied on cell staining, we can identify the antigen distribution on cancer cells by observing the fluorescence. Furthermore, if we use the three scFv simultaneously, we can also detect multiple markers.
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 741
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 451
Illegal NgoMIV site found at 1846 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1762