Difference between revisions of "Part:BBa K533012:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | This plasmid is designed to increase the bio-safety level of biobricks. It contains a constitutive ccdB expression cassette and therefore is toxic to common ''E. coli'' strains. In this way, the spread of this plasmid is restricted. | |
+ | The vector also contains a mutated I-SceI site, which allows for elimation of mutation using our restriction-mutation system. | ||
+ | Do not use commonly used commercial competent cells when using this plasmid. ccdB-resistance strains are required. | ||
===Source=== | ===Source=== |
Revision as of 18:50, 28 October 2011
safety version of pSB1C3 plasmid
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Illegal EcoRI site found at 2590
Illegal XbaI site found at 2596 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2590
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2590
Illegal BamHI site found at 2566
Illegal XhoI site found at 1033
Illegal XhoI site found at 1925 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Illegal suffix found at 2
Illegal EcoRI site found at 2590
Illegal XbaI site found at 2596 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2590
Illegal XbaI site found at 2596
Illegal SpeI site found at 2
Illegal PstI site found at 16 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI.rc site found at 2146
Design Notes
This plasmid is designed to increase the bio-safety level of biobricks. It contains a constitutive ccdB expression cassette and therefore is toxic to common E. coli strains. In this way, the spread of this plasmid is restricted.
The vector also contains a mutated I-SceI site, which allows for elimation of mutation using our restriction-mutation system.
Do not use commonly used commercial competent cells when using this plasmid. ccdB-resistance strains are required.
Source
derived from pSB1C3