Difference between revisions of "Part:BBa K3712008"
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<partinfo>BBa_K3712008 short</partinfo> | <partinfo>BBa_K3712008 short</partinfo> | ||
+ | ===USAGE AND BIOLOGY=== | ||
+ | |||
+ | <p>Verify the thermal aggregation temperature of 27 ELP and the ability of TLR2 antagonist to bind to acylated lipoproteins with the connection of 27ELP and TLR2 antagonist.</p> | ||
+ | |||
+ | ===RESULTS=== | ||
+ | |||
+ | <p>Unfortunately, we have not been able to purify Wild-type TLR2-27 ELP and Optimized TLR2-27 ELP. The results of SDS-PAGE only show the molecular weight of 27 ELP. Therefore, we speculated that passing through the nickel column caused a break between Wild-type/Optimized TLR2 antagonist and 27 ELP.</p> | ||
+ | |||
+ | ===FUTURE DIRECTIONS=== | ||
+ | |||
+ | <p>After we purify the Wild-type/optimized TLR2 antagonist-27 ELP, we will verify that this product has a similar transition temperature with Wild-type BLP-7-27 ELP within ±0.5~1℃.</p> | ||
+ | |||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 13:14, 21 October 2021
Optimized TLR2 antagonist-27 ELP
USAGE AND BIOLOGY
Verify the thermal aggregation temperature of 27 ELP and the ability of TLR2 antagonist to bind to acylated lipoproteins with the connection of 27ELP and TLR2 antagonist.
RESULTS
Unfortunately, we have not been able to purify Wild-type TLR2-27 ELP and Optimized TLR2-27 ELP. The results of SDS-PAGE only show the molecular weight of 27 ELP. Therefore, we speculated that passing through the nickel column caused a break between Wild-type/Optimized TLR2 antagonist and 27 ELP.
FUTURE DIRECTIONS
After we purify the Wild-type/optimized TLR2 antagonist-27 ELP, we will verify that this product has a similar transition temperature with Wild-type BLP-7-27 ELP within ±0.5~1℃.
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 172