Plasmid_Backbone
Part:BBa_J176171
Designed by: Karmella Haynes Group: Haynes Lab (2013-04-19)
Kozak-XbaI-NLS-6His-stop
Mammalian expression vector (without a promoter) designed to add a eukaryotic RBS (Kozak) upstream (in-frame) and a nuclear localization tag (NLS), 6-histidine tag, and stop codon downstream (in-frame) of a protein coding insert. This method only works for Silver Standard (RFC23) inserts.
- Alias: MV9
Usage and Biology
A Promoter Must be Added for Expression
- This vector has no promoter. This design allows the user to customize expression.
- We suggest cutting this vector with SpeI/PstI and inserting a XbaI/PstI-cut promoter into the multiple cloning site (MCS).
- Alternatively, other sites within the MCS to insert a promoter upstream of the Kozak sequence.
Insert a Protein-coding Sequence
- Cut this vector with XbaI. This will open an insertion site between the Kozak and the NLS.
- Dephosphorylate (phosphatase-treat) the vector to prevent self re-ligation.
- Cut your protein-coding insert with XbaI/SpeI.
- The insert must have its XbaI and SpeI sites immediately adjacent to the protein coding sequence.
- The insert must not have a Kozak (RBS) or stop codon.
- Ligate the XbaI/SpeI-cut insert into the XbaI-cut, dephosphorylated vector.
- Pick at least three colonies to increase the likelihood of a forward insert. Since all sticky ends are compatible, the insert can ligate in either direction (forward or reverse). Only forward inserts will express properly.
Should the Promoter be Added First or Second?
- If you want to build a set of plasmids that express different proteins, under control of the same type of promoter, build the Promoter+vector plasmid first
- If you want to build a set of plasmids that express a single protein, under the control of different types of promoters, build the Protein-coding sequence+vector plasmid first
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 266
Illegal XbaI site found at 329
Illegal SpeI site found at 249
Illegal PstI site found at 271 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 266
Illegal SpeI site found at 249
Illegal PstI site found at 271
Illegal NotI site found at 292 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 266
Illegal BglII site found at 12
Illegal XhoI site found at 299 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 266
Illegal XbaI site found at 329
Illegal SpeI site found at 249
Illegal PstI site found at 271 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 266
Illegal XbaI site found at 329
Illegal SpeI site found at 249
Illegal PstI site found at 271
Illegal NgoMIV site found at 819
Illegal NgoMIV site found at 2230 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI.rc site found at 1955
Illegal BsaI.rc site found at 3755
Illegal SapI site found at 2675
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Categories
Parameters
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