Difference between revisions of "Part:BBa K2941001:Design"
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===Design Notes=== | ===Design Notes=== | ||
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− | <p>We modified the original biobrick <a href="https://parts.igem.org/Part:BBa_K567018">BBa_K567018</a> because the strain we used (<i>Eschericia coli</i> C321.deltaA.exp) lacked the T7(1). T7 RNA polymerase is present in a few <i>E. coli</i> strains, but we did not find any of them specifically reprogrammed to be able to incorporate any noncanonical amino acids in TAG codon(2). | + | <p>We modified the original biobrick <a href="https://parts.igem.org/Part:BBa_K567018">BBa_K567018</a> because the strain we used (<i>Eschericia coli</i> C321.deltaA.exp) lacked the T7(1). T7 RNA polymerase is present in a few <i>E. coli</i> strains, but we did not find any of them specifically reprogrammed to be able to incorporate any noncanonical amino acids in TAG codon(2). We added this part to give other teams a reporter that could work in similar settings.</p> |
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Latest revision as of 16:15, 16 October 2019
GFP-TAG-RFP (improved from BBa_K567018)
Assembly Compatibility:
- 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 1302
Illegal AgeI site found at 1414 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
We modified the original biobrick BBa_K567018 because the strain we used (Eschericia coli C321.deltaA.exp) lacked the T7(1). T7 RNA polymerase is present in a few E. coli strains, but we did not find any of them specifically reprogrammed to be able to incorporate any noncanonical amino acids in TAG codon(2). We added this part to give other teams a reporter that could work in similar settings.
Source
This is modified from the biobrick BBa_K567018.
References
1. Escherichia coli C321.deltaA.exp from Addgene. [html document visited 10/09/2019]
2. New England Biolabs. E. coli expression strains. [html document visited 10/09/2019]