Difference between revisions of "PGP888"

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[[File:pGP888.png|250px|thumb|right|'''pGP888: click to enlarge''']]
 
[[File:pGP888.png|250px|thumb|right|'''pGP888: click to enlarge''']]
  
The vector was constructed in the [[Stülke]] lab and it is suitable for the xylose-inducible expression of 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 or NotI  
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The vector was constructed in [[Jörg Stülke]]'s lab and it is suitable for the xylose-inducible expression of 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 or NotI. The plasmid will integrate into the ''[[ganA]]'' gene.
  
  
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*Don't forget a stop codon in the reverse primer.
 
*Don't forget a stop codon in the reverse primer.
  
 
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== The reference ==
 
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<pubmed>21856853 </pubmed>
'''The reference'''
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==  Return to [[Plasmids]] ==
<pubmed> 21856853</pubmed>
 

Latest revision as of 13:59, 3 June 2013

pGP888: click to enlarge

The vector was constructed in Jörg Stülke's lab and it is suitable for the xylose-inducible expression of 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 or NotI. The plasmid will integrate into the ganA gene.


Hints for usage

  • An additional base has to be inserted in the forward primer to restore the frame.
  • Don't forget a stop codon in the reverse primer.

The reference

Return to Plasmids