Reporter
no ATG GFP
Part:BBa_K579000
Designed by: Reo Yoshimura,Toshihiro Matsunami,Takahiro Nakagawa,Jyunpei Yokoigawa Group: iGEM11_KIT-Kyoto (2011-10-05)
no ATG GFP
This plasmid vector was designed to fuse GFP to C-terminal regions of any proteins.(We use BBa_E0240.) In our projects, we use this plasmid to fuse GFP to dMLF, DIAP2, API2-MALT1 and others to monitor expression of these proteins in E. coli and Drosophila.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 641
[edit]
Categories
Parameters
//function/reporter/fluorescence
protein |