Part:BBa_K907004
Dual phase protein generator(GFP default). mRFP and GFP
<Part Description>
This part is derivative of BBa_K907002, twins with BBa_K907005
BBa_E1010(mRFP, reversed) and BBa_E0040(wtGFP) are attached to both ends of BBa_K907002 by overlapping extension PCR. This part normally generates GFP(Left two, figure 1) in E.coli(strain MG1655). When BBa_K907000(Bxb1 integrase) inverts the promoter orientation, it starts to generate mRFP(Right two, figure 1).
<Part Demonstration>
Figure 1. BBa_K907004 in MG1655 expressing GFP or mRFP. Left two: Default state. Center: MG1655 wild-type positive control. Right two: Inverted state.
<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_K907005 - Dual Phase Protein Generator(mRFP default). mRFP and GFP
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 756
Illegal NheI site found at 779 - 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
emission | 511nm(maximum, BBa_E0040), 607nm(maximum, BBa_E1010), 536nm(for detection, BBa_E0040), 619nm(for detection, BBa_E1010) |
excitation | 501nm(BBa_E0040), 584nm(BBa_E1010) |