Device
Part:BBa_K4461500:Design
Designed by: YUAN, HSIAO Group: iGEM22_NYCU-Taipei (2022-10-10)
dusB+RBS+mCeulean+BBa_B0015
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 cloned the promoter from E.coli K-12 MG1655 by PCR. Then we used PCR again to add suffix and prefix. Also, we seperated the plasmid that we want to insert the promoter with two parts. At last, we used gibson assembly to ligate three fragments.
Source
gene synthesis