Plasmid_Backbone
Part:BBa_K2448038:Design
Designed by: jeremy armetta Group: iGEM17_Evry_Paris-Saclay (2017-10-27)
pSB1C3 LacIq
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3218
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 3224 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3218
Illegal XhoI site found at 2202
Illegal XhoI site found at 3094 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found at 3218
Illegal suffix found at 2 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found at 3218
Plasmid lacks a suffix.
Illegal XbaI site found at 3233
Illegal SpeI site found at 2
Illegal PstI site found at 16 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Design Notes
Source
LacIq sequence was amplified by PCR from the pQLinkH vector [1] and inserted using the Golden Gate Assembly technique into the pSB1C3 bearing the BBa_J04450 reporter.
References
[1] Calos MP. DNA sequence for a low-level promoter of the lac repressor gene and an 'up' promoter mutation. Nature (1978) 274, 762-765.
[2] Scheich C, Kümmel D, Soumailakakis D, Heinemann U, Büssow K. Vectors for co-expression of an unrestricted number of proteins. Nucleic Acids Research (2007) 35, e43.