Difference between revisions of "Part:BBa K5401003:Design"
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===Design Notes=== | ===Design Notes=== | ||
The design of the plasmid contains a low-copy number plasmid backbone (BBa_J428341), T7 Promoter (BBa_K3457003), RBS (BBa_J428032), eCFP(BBa_E0020) and T7Terminator (BBa_J428091). | The design of the plasmid contains a low-copy number plasmid backbone (BBa_J428341), T7 Promoter (BBa_K3457003), RBS (BBa_J428032), eCFP(BBa_E0020) and T7Terminator (BBa_J428091). | ||
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===Source=== | ===Source=== | ||
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Molecular cloning using ligation; sequence of individual parts were derived from iGEM Registry. | Molecular cloning using ligation; sequence of individual parts were derived from iGEM Registry. | ||
===References=== | ===References=== |
Latest revision as of 16:03, 1 October 2024
p15A_T7Promoter_eCFP
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 2948
Illegal suffix found in sequence at 16 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 2948
Illegal SpeI site found at 17
Illegal PstI site found at 31
Illegal NotI site found at 24
Illegal NotI site found at 2954 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 2948
- 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 2948
Illegal suffix found in sequence at 17 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 2948
Illegal XbaI site found at 2963
Illegal SpeI site found at 17
Illegal PstI site found at 31
Illegal NgoMIV site found at 1390 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 2188
Design Notes
The design of the plasmid contains a low-copy number plasmid backbone (BBa_J428341), T7 Promoter (BBa_K3457003), RBS (BBa_J428032), eCFP(BBa_E0020) and T7Terminator (BBa_J428091).
Source
Molecular cloning using ligation; sequence of individual parts were derived from iGEM Registry.