Part:pSB1C3:Design

High copy BioBrick assembly plasmid

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  INCOMPATIBLE 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
  
• 21
  INCOMPATIBLE 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
  
• 23
  INCOMPATIBLE WITH RFC[23]

  Illegal prefix found at 2049
  Illegal suffix found at 2
  
• 25
  INCOMPATIBLE 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
  
• 1000
  INCOMPATIBLE WITH RFC[1000]

  Plasmid lacks a prefix.
  Plasmid lacks a suffix.
  

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.

Source

This part was derived from pSB1AC3-P1010.