Difference between revisions of "Part:BBa K907005"
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'''<Part Demonstration>''' | '''<Part Demonstration>''' | ||
− | <br>[[Image: | + | <br>[[Image: KAIST Experimental Results.PNG |center|350px]] |
− | '''Figure 1. | + | '''Figure 1. Experimental results of BBa_K907005.''' Two ep-tubes designated as BBa_K907005 contain centrifuged E.coli MG1655 cells possessing BBa_K907005. When the MG1655-BBa_K907005 is double transformed with <partinfo>BBa_K907000</partinfo>, expressed in pTrcHis2A vector which means under control of Trc promoter, color of cells changed into pink rather than red of MG1655-BBa_K907005. |
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'''<Related Parts>''' | '''<Related Parts>''' |
Revision as of 18:08, 26 September 2012
Dual phase protein generator(mRFP default). mRFP and GFP
<Part Description>
This part is derivative of BBa_K907003, twins with BBa_K907005
BBa_E1010(mRFP, reversed) and BBa_0040(wtGFP) are attached to both ends of BBa_K907003 by overlapping extension PCR. This part normally generates mRFP in E.coli(strain MG1655). When BBa_K907000(Bxb1 integrase) inverts the promoter orientation, it starts to generate GFP.
<Part Demonstration>
Figure 1. Experimental results of BBa_K907005. Two ep-tubes designated as BBa_K907005 contain centrifuged E.coli MG1655 cells possessing BBa_K907005. When the MG1655-BBa_K907005 is double transformed with BBa_K907000, expressed in pTrcHis2A vector which means under control of Trc promoter, color of cells changed into pink rather than red of MG1655-BBa_K907005.
<Related Parts>
BBa_K907000 - Mycobacterium Phage Bxb1 integrase
BBa_K907001 - Mycobacterium Phage Bxb1 excisionase
BBa_K907002 - Binary Signal Generator, RBS(reverse) - attB - Promoter - attP - RBS
BBa_K907003 - Binary Signal Generator, Promoter Reversed, RBS(reverse) - attB - Promoter(reverse) - attP - RBS
BBa_K907004 - Dual Phase Protein Generator(GFP default). mRFP and GFP
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 750
Illegal NheI site found at 773 - 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 838
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 703
Illegal AgeI site found at 10
Illegal AgeI site found at 122 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 723
Illegal BsaI.rc site found at 806
Illegal BsaI.rc site found at 1499