Difference between revisions of "Part:BBa K3765011"
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<partinfo>BBa_K3765011 short</partinfo> | <partinfo>BBa_K3765011 short</partinfo> | ||
− | High copy number vector | + | High copy number KanR vector which can be used for expression under a strong T7 promoter. The promoter, operator, RBS and terminator are already included in the plasmid, so any CDS can be cloned into the MCS and be ready to express. |
− | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | This vector was used in our project to clone and express all of our constructs coding for fusion proteins. | ||
+ | ---- | ||
− | |||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K3765011 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3765011 SequenceAndFeatures</partinfo> |
Latest revision as of 07:05, 21 October 2021
pETMCN-T7
High copy number KanR vector which can be used for expression under a strong T7 promoter. The promoter, operator, RBS and terminator are already included in the plasmid, so any CDS can be cloned into the MCS and be ready to express.
Usage and Biology
This vector was used in our project to clone and express all of our constructs coding for fusion proteins.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 5105
Illegal SpeI site found at 5030 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 5111
Illegal SpeI site found at 5030 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 4964
Illegal BamHI site found at 5093
Illegal XhoI site found at 5075 - 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 5105
Illegal SpeI site found at 5030 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 5105
Illegal SpeI site found at 5030
Illegal NgoMIV site found at 137
Illegal NgoMIV site found at 3184
Illegal NgoMIV site found at 3344
Illegal NgoMIV site found at 4932 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 2263