Difference between revisions of "Part:BBa K3187008"
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<h1>Results</h1> | <h1>Results</h1> | ||
− | + | For results regarding this part, please have a look at <a href="https://parts.igem.org/Part:BBa_K3187028" | |
+ | target="_blank">(BBa_K3187028)</a> | ||
</html> | </html> | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 15:56, 21 October 2019
GGGG-Tag for Sortase-mediated Ligation x mCherry Fluorescence Protein
Profile
Name | GGGG-mCherry |
Base pairs | 1028 |
Molecular weight | 28.5 kDa |
Origin | synthetic, derived from Discosoma sp. |
Parts | mCherry, GGGG-sequence, T7 Promoter, lac Operator, GASPAG Linker, Strep-Tag II, T7 Terminator |
Properties | Red fluorescent, Ex λ: 587nm, Em λ: 610 nm |
Usage and Biology
mCherry (BBa_K3187026) is a red
fluorescent
protein.
Which is a synthetic protein derived from Discosoma sp. by
directed evolution. The N-terminal GGGG-sequence (BBa_K3187018)
can be fused to a protein with a C-terminal LPETGG-Sortase A link (BBa_K3187019)
by Sortase A. We use mCherry as an easily imaged reporter for checking if the coupling worked.
The coding sequence was cloned in pET24 vector, containing the sequence of mCherry, a
GGGG-sequence, a GASPAG Linker
(BBa_K3187038), a
Strep-Tag II (BBa_K3187025)
for
Purification, a T7 Promoter with lac Operator and an RBS (BBa_K3187029), a T7 Terminator (BBa_K3187032), a Start-Codon (BBa_J70593)
and a Stop-Codon (BBa_K2868029). The
coding sequence consists of 851 bp which are translated to 260 amino acids.[1]
Results
For results regarding this part, please have a look at (BBa_K3187028) Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 854
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 854
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 915
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 854
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 854
- 1000COMPATIBLE WITH RFC[1000]