Difference between revisions of "Part:BBa K165060"
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Original Sikorski vector was described in R. S. Sikorski and P. Hieter, Genetics, 122: 19-27 (1989). | Original Sikorski vector was described in R. S. Sikorski and P. Hieter, Genetics, 122: 19-27 (1989). | ||
− | [http://www.genetics.org/cgi/reprint/122/1/19.pdf | + | [http://www.genetics.org/cgi/reprint/122/1/19.pdf Original Paper] |
Revision as of 05:50, 30 October 2008
pRS303 yeast shuttle vector, HIS3
Ampicillin resistance when grown in bacteria. This plasmid is not currently Biobrick compatible, but is useful for inserting a final construct into a yeast cell.
Useful for chromosomal integration of a device into yeast strains. This will insert the vector at the specific locus of the HIS3 gene. To be used in conjunction with histidine drop-out media for positive selection of transformed cells. Transformation using this vector requires linearization of the plasmid by cutting with PstI.
To incorporate a single Biobrick part into this vector for subsequent transformation into yeast, one should cut both vector and part with EcoRI and SpeI.
Alternatively, one can do the final ligation step between two Biobrick parts into this vector by cutting with the following:
Vector: EcoRI, Not I
Prefix: EcoRI, SpeI
Suffix: XbaI, NotI
Original Sikorski vector was described in R. S. Sikorski and P. Hieter, Genetics, 122: 19-27 (1989). [http://www.genetics.org/cgi/reprint/122/1/19.pdf Original Paper]
Yeast transformation protocol:
R Daniel Gietz & Robert H Schiestl. High-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method . Nature protocols (2007)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 2127
Illegal XbaI site found at 2097
Illegal SpeI site found at 2103
Illegal PstI site found at 1182
Illegal PstI site found at 2121 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 2127
Illegal NheI site found at 1007
Illegal SpeI site found at 2103
Illegal PstI site found at 1182
Illegal PstI site found at 2121
Illegal NotI site found at 2089 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 2127
Illegal BglII site found at 898
Illegal BglII site found at 958
Illegal BamHI site found at 2109
Illegal XhoI site found at 2160 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 2127
Illegal XbaI site found at 2097
Illegal SpeI site found at 2103
Illegal PstI site found at 1182
Illegal PstI site found at 2121 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 2127
Illegal XbaI site found at 2097
Illegal SpeI site found at 2103
Illegal PstI site found at 1182
Illegal PstI site found at 2121
Illegal NgoMIV site found at 1748 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 3533
Illegal SapI site found at 2450