Plasmid_Backbone
Part:BBa_K731700
Designed by: Giacomo Giacomelli, Anna Depetris Group: iGEM12_UNITN-Trento (2012-08-14)
Platform for terminators analysis under the control of T7 promoter
This part is used to analyse terminators: two subsequent fluorescent proteins (mCherry and A206K Venus), separated by Prefix-Suffix linker, allow standardization of terminator's presence effect. The vector is a modified pET21b; it contains Ampicillin resistance gene and is inducible by IPTG (T7promoter-lacO).
The combined use of Part:BBa_K731710 and BBa_K731700 allow also to analyse any potential difference in terminators' activity due to different polymerases.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 6850
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 6856 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 6850
Illegal BglII site found at 6011
Illegal BamHI site found at 6832
Illegal XhoI site found at 753 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found at 6850
Illegal suffix found at 2 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found at 6850
Plasmid lacks a suffix.
Illegal XbaI site found at 6865
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NgoMIV site found at 714
Illegal NgoMIV site found at 1051
Illegal NgoMIV site found at 4231
Illegal NgoMIV site found at 4391
Illegal NgoMIV site found at 5979
Illegal AgeI site found at 6800 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI site found at 2228
Illegal SapI.rc site found at 3310
[edit]
Categories
Parameters
//chassis/bacteriophage/t7
//plasmid/measurement
//plasmid/measurement
None |