Plasmid_Backbone
Part:BBa_K106698:Design
Designed by: Andrew Horwitz Group: iGEM08_UCSF (2008-10-29)
AarI AD acceptor vector (pRS315, 8X LexAOps Fig1P, Adh1t)
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 6244 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 6244
Illegal NotI site found at 4048 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 6244
Illegal BamHI site found at 4031
Illegal XhoI site found at 3965
Illegal XhoI site found at 4950 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 6244 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 6244
Illegal NgoMIV site found at 3133
Illegal NgoMIV site found at 4561
Illegal AgeI site found at 5857 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI site found at 1430
Illegal SapI.rc site found at 408
Illegal SapI.rc site found at 2512
Design Notes
LexA Ops were cloned non-directionally into the PspOMI site. Inner site is broken, thus the cassette can be subcloned from this plasmid by PspOMI/SacI digestion (for example, to change markers).
Source
Modification of the AarI AD acceptor vector (pRS315, Cyc1P, Adh1t).