Difference between revisions of "Part:BBa K5301018"
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− | Figure 1.PCR result of the | + | Figure 1.PCR result of the sGFP11 tether.The base sequence length of the sGFP11 tether is 477 base pairs (bp) |
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Revision as of 08:35, 1 October 2024
sGFP11 tether is composed of mSA, a 3C linker, a 6His tag, and sGFP 11.
sGFP11 tether is composed of mSA, a 3C linker, a 6�His tag, and sGFP 11.We construct membrane protein dimers through the interaction between biotin and streptavidin, as well as the self-assembly mechanism of sGFP.
Usage and Biology
mSA is used for binding to biotinylated proteins, and sGFP1-10 and sGFP11 self-assemble to form GFP, thereby creating a protein dimer that can report the outcome with fluorescence.
Characterization
PCR
We conducted colony PCR validation to assess the feasibility of the plasmid pathway, as shown in Figure 1, where the corresponding bands are very clear, indicating that the target fragments were successfully introduced into the plasmid and transformed into the bacterial strain.
SDS-PAGE
SDS-PAGE was used to verify the purification of the sGFP11 tether. Due to the particularity of mSA, we simultaneously purified the soluble proteins from the supernatant and the inclusion body proteins from the pellet after bacterial lysis. It can be observed that the concentration and purity of the purified inclusion body proteins are high, while the concentration of the soluble proteins is low. Further exploration of soluble protein expression or assessment of inclusion body protein activity can be conducted subsequently. Based on the experience with the sGFP1-10 tether, we have purified the soluble and inclusion body proteins of the sGFP11 tether, as shown in Figure 2.
ELISA
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 82
Illegal AgeI site found at 142 - 1000COMPATIBLE WITH RFC[1000]