From Tol2Kit
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=== Construction details === | === Construction details === | ||
− | p5E-MCS was made by PCR of the pBSII SK+ multiple cloning site, from T7 to T3 primers, followed by a BP reaction. Sequencing confirms that all bases of the insert are correct. | + | p5E-MCS was made by PCR of the pBSII SK+ multiple cloning site, from T7 to T3 primers, followed by a BP reaction with pDONR P4-P1R. Sequencing confirms that all bases of the insert are correct. |
+ | |||
+ | M13F, M13R, and T3 should all work as sequencing primers. | ||
+ | |||
+ | Unfortunately, the backbone of P4-P1R contains recognition sites for several potentially useful restriction enzymes. The restriction sites from the Bluescript MCS that remain unique in p5E-MCS are: | ||
+ | |||
+ | ''Asp718-KpnI-DraII-XhoI-SalI-Bsp106-HindIII-SmaI-BamHI-SpeI-SacII-BstXI'' | ||
+ | |||
+ | === Sequence === | ||
+ | Annotated sequence, Genbank format:<br> | ||
+ | [[p5E-MCS Genbank]] | ||
− | |||
FASTA file with the full-length sequence as well as sequences of individual components:<br> | FASTA file with the full-length sequence as well as sequences of individual components:<br> | ||
[[p5E-MCS sequence]] | [[p5E-MCS sequence]] |
Latest revision as of 03:43, 19 December 2007
Construction details
p5E-MCS was made by PCR of the pBSII SK+ multiple cloning site, from T7 to T3 primers, followed by a BP reaction with pDONR P4-P1R. Sequencing confirms that all bases of the insert are correct.
M13F, M13R, and T3 should all work as sequencing primers.
Unfortunately, the backbone of P4-P1R contains recognition sites for several potentially useful restriction enzymes. The restriction sites from the Bluescript MCS that remain unique in p5E-MCS are:
Asp718-KpnI-DraII-XhoI-SalI-Bsp106-HindIII-SmaI-BamHI-SpeI-SacII-BstXI
Sequence
Annotated sequence, Genbank format:
p5E-MCS Genbank
FASTA file with the full-length sequence as well as sequences of individual components:
p5E-MCS sequence