Difference between revisions of "PGP380"

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[[File:PGP380_cloning_region.jpeg|250px|thumb|right|'''pGP380 cloning region: click to enlarge''']]
 
[[File:PGP380_cloning_region.jpeg|250px|thumb|right|'''pGP380 cloning region: click to enlarge''']]
  
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Vector for the overexpression of N-terminally Strep-tagged proteins in ''B. subtilis'', used for the [[SPINE]] technology
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The vector was constructed in the [[Stülke]] lab and it is suitable for constitutive overexpression of N-terminally Strep-tagged proteins in ''B. subtilis''. The plasmid confers resistance to ampicillin and erythromycin in ''E. coli'' and ''B. subtilis'', respectively. pGP380 can be used for the [[SPINE]] method. [[pGP382]] is similar to the vector pGP380 which is based on the vectors [[pBQ200]] and [[pHT315]].
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constructed in [[Stülke]] lab
 
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in ''E. coli'': ampicillin resistance
 
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in ''B. subtilis'': erythromycin resistance
 
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based on [[pBQ200]]
 
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similar vector: [[pGP382]]
 
  
 
sequencing primer:  
 
sequencing primer:  

Revision as of 12:47, 25 February 2010

pGP380: click to enlarge
pGP380 cloning region: click to enlarge

The vector was constructed in the Stülke lab and it is suitable for constitutive overexpression of N-terminally Strep-tagged proteins in B. subtilis. The plasmid confers resistance to ampicillin and erythromycin in E. coli and B. subtilis, respectively. pGP380 can be used for the SPINE method. pGP382 is similar to the vector pGP380 which is based on the vectors pBQ200 and pHT315.

sequencing primer:

  • M13_puc_for: 5‘-GTAAAACGACGGCCAGTG-3‘
  • M13_puc_rev: 5‘-GGAAACAGCTATGACCATG-3‘


Christina Herzberg, Lope Andrés Flórez Weidinger, Bastian Dörrbecker, Sebastian Hübner, Jörg Stülke, Fabian M Commichau
SPINE: a method for the rapid detection and analysis of protein-protein interactions in vivo.
Proteomics: 2007, 7(22);4032-5
[PubMed:17994626] [WorldCat.org] [DOI] (P p)