Plasmid_Backbone
Part:BBa_K3425014:Design
Designed by: Núria Garriga Alonso Group: iGEM20_UofUppsala (2020-10-19)
pSB4A02: pOdd2 Loop Vector based on pSB4A5
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3404
Illegal PstI site found at 12 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3404
Illegal PstI site found at 12 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3404 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3404
Illegal PstI site found at 12 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3404
Illegal PstI site found at 12 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal SapI site found at 3410
Illegal SapI.rc site found at 5
Design Notes
pOdd2 Loop Vector based on pSB4A5 for level 3 assemblies. A Gibson assembly experiment was designed, using three parts amplified via PCR:
- The mRFP1 device (BBa_J04454) from pSB1K02 with VF2 and VR primers
- Part of the pSB4A5 sequence with GIBSON_3K#1_Rv_4A#1_Fw and GIBSON_4A#1_Rv_4K#1_Rv primers
- Part of the pSB4A5 sequence with GIBSON_4A#2_Fw_4K#2_Fw and GIBSON_3K#2_Fw_4A#2_Rv_4K#1_Fw primers
Source
Gibson assembly from parts of pSB4A5 and BBa_J04454.