Difference between revisions of "PGP1460"
| Line 10: | Line 10: | ||
Sequencing primers: | Sequencing primers: | ||
| − | *''' | + | *'''KG64:''' 5‘-TATCAGGGCCTCGACTACA-3‘ |
| − | *''' | + | *'''ML107:''' 5‘-GCTTCATAGAGTAATTCTGTAAAGG-3‘ |
Similar plasmid: [[pGP1459]] (for N-terminal Strep-tags) | Similar plasmid: [[pGP1459]] (for N-terminal Strep-tags) | ||
<pubmed> </pubmed> | <pubmed> </pubmed> | ||
Revision as of 13:46, 2 May 2013
The vector was constructed in the Stülke lab and it is suitable for constitutive expression of C-terminally Strep-tagged proteins in B. subtilis. The plasmid confers resistance to ampicillin and kanamycin in E. coli and B. subtilis, respectively. To transform B. subtilis, the plasmid has to be linearized with ScaI. The plasmid will integrate into the ganA gene. Just like pGP382 it can be used for the SPINE method.
The cloning region of pGP382 is shown for detailed information.
Genes cloned into this vector require a Shine-Dalgarno sequence.
Sequencing primers:
- KG64: 5‘-TATCAGGGCCTCGACTACA-3‘
- ML107: 5‘-GCTTCATAGAGTAATTCTGTAAAGG-3‘
Similar plasmid: pGP1459 (for N-terminal Strep-tags)
