Difference between revisions of "Part:BBa K2398559:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | + | This part was created from the wildtype <i>E.coli</i> beta-glucuronidase. One or more amino acid substitutions were introduced. It was used for protein expression under a lac inducible T7 promoter. | |
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===Source=== | ===Source=== | ||
| − | + | This part was modified from the beta-glucuronidase coding sequence of <i>E. coli</i>, obtained from AddGene (#61156). | |
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===References=== | ===References=== | ||
Latest revision as of 13:45, 1 November 2017
Beta-Glucuronidase_T509A
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 506
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part was created from the wildtype E.coli beta-glucuronidase. One or more amino acid substitutions were introduced. It was used for protein expression under a lac inducible T7 promoter.
Source
This part was modified from the beta-glucuronidase coding sequence of E. coli, obtained from AddGene (#61156).