![](https://parts.igem.org/images/partbypart/icon_plasmid_backbone.png)
Plasmid_Backbone
Part:BBa_K5299006:Design
Designed by: Maria Nefeli Stoupa Group: iGEM24_Thessaly (2024-09-24)
Tn7-M: KmR GmR, ori R6K, Tn7L and Tn7R extremes, standard multiple cloning site
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 56
Illegal XbaI site found at 83
Illegal SpeI site found at 145
Illegal PstI site found at 95 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 56
Illegal SpeI site found at 145
Illegal PstI site found at 95
Illegal NotI site found at 46
Illegal NotI site found at 113 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 56
Illegal BglII site found at 411
Illegal BglII site found at 2606
Illegal BamHI site found at 77 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 56
Illegal XbaI site found at 83
Illegal SpeI site found at 145
Illegal PstI site found at 95 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 56
Illegal XbaI site found at 83
Illegal SpeI site found at 145
Illegal PstI site found at 95
Illegal NgoMIV site found at 1645
Illegal NgoMIV site found at 1649 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Design Notes
R6K origin of replication requires a pir strain for replication
Source
Mini-Tn7 vectors have been developed and proven to be useful for integration of a cloned gene and genetic analysis of several Gram-