Part:BBa_K165063
pRS306 yeast shuttle vector, URA3 selection
Useful for chromosomal integration of a part into yeast strains. Insertion of a single Biobrick (or biofusion) part requires cutting with EcoRI and SpeI. Another option for this vector is to insert two Biobrick/biofusion parts by cutting the first part with NotI and SpeI and the second part with XbaI and PstI, while cutting the vector with NotI and PstI. Note that this part does not conform to Standard Assembly requirements and will maintain idempotency. Once a construct of interest has been inserted into the vector, it should be linearized with a digest using PstI. This vector will supplement a URA3 auxotrophic yeast strain. The part is then transformed into yeast according to the protocol outlined in this paper:
R Daniel Gietz & Robert H Schiestl. High-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method . Nature protocols
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 2047
Illegal XbaI site found at 2017
Illegal SpeI site found at 2023
Illegal PstI site found at 389
Illegal PstI site found at 2041 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 2047
Illegal SpeI site found at 2023
Illegal PstI site found at 389
Illegal PstI site found at 2041
Illegal NotI site found at 2009 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 2047
Illegal BamHI site found at 2029
Illegal XhoI site found at 2080 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 2047
Illegal XbaI site found at 2017
Illegal SpeI site found at 2023
Illegal PstI site found at 389
Illegal PstI site found at 2041 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 2047
Illegal XbaI site found at 2017
Illegal SpeI site found at 2023
Illegal PstI site found at 389
Illegal PstI site found at 2041
Illegal NgoMIV site found at 1668 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1079
Illegal BsaI.rc site found at 3453
Illegal SapI site found at 2370
Illegal SapI.rc site found at 926
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