Difference between revisions of "Part:BBa K133015"
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<partinfo>BBa_K133015 short</partinfo> | <partinfo>BBa_K133015 short</partinfo> | ||
− | CF215 is the C-terminal portion of chimeric fusion protein; it contains the C-terminal segment of the hypervariable region of H. pylori flagellin FlaA from 215 AA + 99 AA of C-terminal portion from E. coli flagellin; useful for inserting protein segments into the chimeric flagellin (example: CF213-multiepitope-CF215). In combination with CF213 it forms a TLR5 activating protein. | + | CF215 is the C-terminal portion of chimeric fusion protein; it contains the C-terminal segment of the hypervariable region of <i>H. pylori</i> flagellin FlaA from 215 AA + 99 AA of C-terminal portion from <i>E. coli</i> flagellin; useful for inserting protein segments into the chimeric flagellin (example: CF213-multiepitope-CF215). In combination with CF213 it forms a TLR5 activating protein. |
mCherry is a red fluorescent protein that can be used for localisation studies. | mCherry is a red fluorescent protein that can be used for localisation studies. | ||
+ | |||
+ | Since the protein was designed to be produced, we additionally added RGD-Hisstop tag. | ||
Latest revision as of 05:06, 30 October 2008
CF215-mCherry-RGD-Histop
CF215 is the C-terminal portion of chimeric fusion protein; it contains the C-terminal segment of the hypervariable region of H. pylori flagellin FlaA from 215 AA + 99 AA of C-terminal portion from E. coli flagellin; useful for inserting protein segments into the chimeric flagellin (example: CF213-multiepitope-CF215). In combination with CF213 it forms a TLR5 activating protein.
mCherry is a red fluorescent protein that can be used for localisation studies.
Since the protein was designed to be produced, we additionally added RGD-Hisstop tag.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 571
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 128
Illegal BamHI site found at 639
Illegal BamHI site found at 1603 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1638