Part:BBa_K1680014:Design
pRS313 yeast shuttle vector with Biobrick MCS
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2120
Illegal XbaI site found at 2105
Illegal SpeI site found at 2097
Illegal PstI site found at 2083 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2120
Illegal NheI site found at 1007
Illegal SpeI site found at 2097
Illegal PstI site found at 2083
Illegal NotI site found at 2088
Illegal NotI site found at 2112 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2120
Illegal BglII site found at 898
Illegal BglII site found at 958 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2120
Illegal XbaI site found at 2105
Illegal SpeI site found at 2097
Illegal PstI site found at 2083 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2120
Illegal XbaI site found at 2105
Illegal SpeI site found at 2097
Illegal PstI site found at 2083
Illegal NgoMIV site found at 1748 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI.rc site found at 3494
Illegal SapI site found at 2411
Illegal SapI site found at 4515
Design Notes
This part is derived from the pRS313 vector (Sikorski 1989). It is mutagenised to be compatible with RFC10 and the wild type MCS was switched for a RFC10 MCS. The biobrick MCS is flanked by ApaI (Prefix) and SacI (Suffix) restriction sites. These can be used together with either EcoRI or PstI site to introduce a promoter or terminator stably into the vector without disturbing the RFC10 standard.
Sequence of the new RFC10 MCS:
GGGCCCACGTGAATTCGCGGCCGCTTCTAGAGTACTAGTAGCGGCCGCTGCAGACGTGAGCTC
Source
Derived from pRS313 Part:BBa_K950008 (Sikorski 1989).
References
Sikorski, Robert S., and Philip Hieter. "A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae." Genetics 122.1 (1989): 19-27.