Difference between revisions of "Part:BBa K2762001:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | We first codon optimized the rbcX sequence and sent it to IDT for gene synthesis. The gene fragment is amplified via PCR reaction for cloning. | + | We first codon optimized the rbcX sequence and sent it to IDT for gene synthesis. The gene fragment is amplified via PCR reaction for cloning. |
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===Source=== | ===Source=== | ||
| − | + | Codon oprimized <i>Synechococcus elongatus</i> PCC7002. | |
===References=== | ===References=== | ||
Latest revision as of 13:31, 12 October 2018
Assembly chaperone of ribulose-bisphosphate carboxylase/oxygenase rbcX
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We first codon optimized the rbcX sequence and sent it to IDT for gene synthesis. The gene fragment is amplified via PCR reaction for cloning.
Source
Codon oprimized Synechococcus elongatus PCC7002.