Difference between revisions of "Part:BBa K103019"
| Line 11: | Line 11: | ||
*Prey protein should be attached via linker (using BamHI+ Biobrick standard suffix enzyme). | *Prey protein should be attached via linker (using BamHI+ Biobrick standard suffix enzyme). | ||
*Fusion protein can be purified on NiNTA bead (tkanks to presence of N-terminal His-Tag). | *Fusion protein can be purified on NiNTA bead (tkanks to presence of N-terminal His-Tag). | ||
| + | *Generator under control of T7 promoter | ||
*Interaction between hunter and prey added to the medium makes cells ampicillin resistant | *Interaction between hunter and prey added to the medium makes cells ampicillin resistant | ||
*This part uses our NdeI/SacI/BamHI fusion cloning substandard | *This part uses our NdeI/SacI/BamHI fusion cloning substandard | ||
Latest revision as of 12:54, 28 October 2008
alpha_linker under PT7
Usage and Biology
- Construct for creating prey fusions for our 'hunter and prey' selection system
- Fusion partners are connected via Gly-Ser-Gly linker
- Prey protein should be attached via linker (using BamHI+ Biobrick standard suffix enzyme).
- Fusion protein can be purified on NiNTA bead (tkanks to presence of N-terminal His-Tag).
- Generator under control of T7 promoter
- Interaction between hunter and prey added to the medium makes cells ampicillin resistant
- This part uses our NdeI/SacI/BamHI fusion cloning substandard
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]
- 1000COMPATIBLE WITH RFC[1000]