Difference between revisions of "Part:BBa K4361103"
Line 3: | Line 3: | ||
<partinfo>BBa_K4361103 short</partinfo> | <partinfo>BBa_K4361103 short</partinfo> | ||
− | + | Composite part consisting of <i>E. coli</i> codon optimized BlcR ([[Part:BBa_K4361100]], with a His-tag for purification and TEV cleavage site for separation of said tag from the protein ([[Part:BBa_K4361104]]). Through this combination, we were able to attain improved expression of our protein of interest and subsequently purify it without inhibiting its functionality. | |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
Line 9: | Line 9: | ||
<!-- --> | <!-- --> | ||
− | <span class='h3bb'>Sequence and Features</span> | + | <span class='h3bb'><h3>Sequence and Features</h3></span> |
<partinfo>BBa_K4361103 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4361103 SequenceAndFeatures</partinfo> | ||
Revision as of 08:17, 11 October 2022
BlcR with 6xHis-tag and TEV protease cleavage site
Composite part consisting of E. coli codon optimized BlcR (Part:BBa_K4361100, with a His-tag for purification and TEV cleavage site for separation of said tag from the protein (Part:BBa_K4361104). Through this combination, we were able to attain improved expression of our protein of interest and subsequently purify it without inhibiting its functionality.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 766
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 901
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 150
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 661