Difference between revisions of "PGP1459"
(Created page with "The vector was constructed in the Stülke lab and it is suitable for constitutive expression of N-terminally Strep-tagged proteins in ''B. subtilis''. The plasmid confers res...") |
|||
(8 intermediate revisions by 5 users not shown) | |||
Line 1: | Line 1: | ||
− | The vector was constructed in the [[Stülke]] lab and it is suitable for constitutive expression of N-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. Just like pGP380 it can be used for the [[SPINE]] method. | + | [[File:PGP1459.png|250px|thumb|right|'''PGP1459: click to enlarge''']] |
+ | [[File:PGP380_cloning_region.jpeg|250px|thumb|right|'''pGP380 cloning region: click to enlarge''']] | ||
+ | |||
+ | The vector was constructed in the [[Stülke]] lab and it is suitable for constitutive expression of N-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 [[pGP380]] it can be used for the [[SPINE]] method. | ||
+ | |||
+ | The cloning region of [[pGP380]] is shown for detailed information. | ||
+ | |||
Sequencing primers: | Sequencing primers: | ||
− | *''' | + | *'''KG64:''' 5‘-TATCAGGGCCTCGACTACA-3‘ |
− | *''' | + | *'''ML107:''' 5‘-GCTTCATAGAGTAATTCTGTAAAGG-3‘ |
+ | |||
+ | Similar plasmid: [[pGP1460]] (for C-terminal Strep-tags) | ||
+ | <pubmed> 23192352 </pubmed> | ||
− | + | == Return to [[Plasmids]] == |
Latest revision as of 13:58, 3 June 2013
The vector was constructed in the Stülke lab and it is suitable for constitutive expression of N-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 pGP380 it can be used for the SPINE method.
The cloning region of pGP380 is shown for detailed information.
Sequencing primers:
- KG64: 5‘-TATCAGGGCCTCGACTACA-3‘
- ML107: 5‘-GCTTCATAGAGTAATTCTGTAAAGG-3‘
Similar plasmid: pGP1460 (for C-terminal Strep-tags)