Difference between revisions of "Part:pSB1C3:Design"
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===Original Sequence=== | ===Original Sequence=== | ||
− | In Spring 2011, pSB1C3 was sequenced using several primers. The current sequence reflects the most recent sequencing of pSB1C3 (w/ BBa_J04450, located in SP 4000 Well 2A). | + | In Spring 2011, pSB1C3 was sequenced using several primers. The current sequence reflects the most recent sequencing of pSB1C3 (w/ BBa_J04450, located in SP 4000 Well 2A). However for posterity, we have included images of the original sequence with markers pointing out the changes made: [[Image:PSB1C3-Text-Archival-5-4-11.txt]] |
[[Image:PSB1C3-Seq-Archival-5-4-11.png|300px]] | [[Image:PSB1C3-Seq-Archival-5-4-11.png|300px]] |
Revision as of 19:40, 4 May 2011
High copy BioBrick assembly plasmid
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2049
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 2055 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2049
Illegal XhoI site found at 1033
Illegal XhoI site found at 1925 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found at 2049
Illegal suffix found at 2 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found at 2049
Plasmid lacks a suffix.
Illegal XbaI site found at 2064
Illegal SpeI site found at 2
Illegal PstI site found at 16 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Original Sequence
In Spring 2011, pSB1C3 was sequenced using several primers. The current sequence reflects the most recent sequencing of pSB1C3 (w/ BBa_J04450, located in SP 4000 Well 2A). However for posterity, we have included images of the original sequence with markers pointing out the changes made: File:PSB1C3-Text-Archival-5-4-11.txt
Design Notes
Eliminated ampicillin resistance.
Subversions
Freiburg's pSB1C3 varient of 2010
The iGEM team Freiburg created a modified version of the pSB1C3 in which the two restriction sites SspI and PvuII were removed via site directed mutagenesis. These restriction sites and two others that are not present in the pSB1C3 (BamHI and SalI) were used as single cutting restriction sites to replace the loop coding sequences of the Adeno-associated Virus. For this purpose scar-less cloning is necessary, because of the unpredictable consequences on the viral vector performance arising from mutations or insertions. The final capsid gene adheres fully to the RFC_10 standard.
The sequence and a more detailled description can be found under the BioBrick ID BBa_K404200.
Source
This part was derived from pSB1AC3-P1010.