Difference between revisions of "Part:pSB1T3:Design"
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The ampicillin resistance marker needed to be eliminated. | The ampicillin resistance marker needed to be eliminated. | ||
− | + | Based on conversation with Austin Che, I believe the Tet marker in this plasmid was cloned in a non-directional fashion between two XhoI sites. As a result, the Tet marker in the Registry version of this plasmid could be in either orientation. Sequencing of the Registry clone would confirm which orientation is present. | |
===Source=== | ===Source=== |
Latest revision as of 18:53, 5 February 2013
High copy BioBrick assembly plasmid
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2440
Illegal NheI site found at 1268
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 2446 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2440
Illegal BamHI site found at 1414
Illegal XhoI site found at 1033
Illegal XhoI site found at 2316 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found at 2440
Illegal suffix found at 2 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found at 2440
Plasmid lacks a suffix.
Illegal XbaI site found at 2455
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NgoMIV site found at 1440
Illegal NgoMIV site found at 1808
Illegal NgoMIV site found at 1968 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Design Notes
The ampicillin resistance marker needed to be eliminated.
Based on conversation with Austin Che, I believe the Tet marker in this plasmid was cloned in a non-directional fashion between two XhoI sites. As a result, the Tet marker in the Registry version of this plasmid could be in either orientation. Sequencing of the Registry clone would confirm which orientation is present.
Source
Austin Che constructed this plamid from pSB1AT3-P1010.