Plasmid_Backbone
Part:BBa_K289008
Designed by: Nan Hou Group: iGEM09_Tianjin (2009-10-21)
PGBKT7(YEAST PLASMIDE BACKBONE)
The pGBKT7 vevtor expresses proteins fused to amino acids of the GAL4 DNA binding domain(DNA-BD).In yeast ,fusion proteins are expressed at high levels from the constitutive ADH1 promoter ;transcription is terminated by the T7 and ADH1 transcription termination signials. pGBKT7 also contains the T7 promoter, a c-Myc epitope tag, and a MCS. pGBKT7 replicates autonomously in both E.coli and S.cerevisiae from the pUC and 2μ ori, respectively. The vector carries the Kan for selection in E.coli and the TRP1 nutritional marker for selection in yeast. Yeast strains containing pGBKT7 exhibit a higher transformation efficiency than strains carrying other DNA-BD domain vectors.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 1299
Illegal XbaI site found at 5126
Illegal XbaI site found at 6114
Illegal PstI site found at 1321 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 1299
Illegal PstI site found at 1321
Illegal NotI site found at 1326 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 1299
Illegal BamHI site found at 1309
Illegal XhoI site found at 979 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 1299
Illegal XbaI site found at 5126
Illegal XbaI site found at 6114
Illegal PstI site found at 1321 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 1299
Illegal XbaI site found at 5126
Illegal XbaI site found at 6114
Illegal PstI site found at 1321
Illegal NgoMIV site found at 3099
Illegal NgoMIV site found at 3383
Illegal NgoMIV site found at 7133 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI site found at 119
Illegal BsaI site found at 898
Illegal BsaI site found at 2887
Illegal SapI site found at 1841
Illegal SapI site found at 3323
Illegal SapI site found at 3533
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Categories
Parameters
None |