Difference between revisions of "PGP1331"

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(Created page with ' '''general comments''' Integrative Plasmid for the fusion of 3x FLAG tag to the C-terminus of a protein, keeping the control of the expression under its natural promotor E.col…')
 
 
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[[File:PGP1331.png|250px|thumb|right|'''pGP1331: click to enlarge''']]
  
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'''General comments'''
  
'''general comments'''
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Integrative [[plasmid]] for the fusion of 3x FLAG tag to the C-terminus of a protein, keeping the control of the expression under its natural promotor
 
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* ''E.coli'': multicopy plasmid, select for ampicillin
Integrative Plasmid for the fusion of 3x FLAG tag to the C-terminus of a protein, keeping the control of the expression under its natural promotor
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* ''B. subtilis'': no ori, select for spectinomycin
E.coli: multicopy plasmid, select for ampicillin
 
B. subtilis: no ori, select for spectinomycin
 
  
 
'''Hints for the usage'''
 
'''Hints for the usage'''
amplify the last 600bp of your gene of interest,  
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* amplify the last 600bp of your gene of interest,  
skip the Stopp-Codon of the gene in the revers primer
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* skip the Stop-codon of the gene in the reverse primer
take care that the integration is in-frame
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* take care that the integration is in-frame
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* Don't use XbaI and KpnI for cloning. They cut the vector twice!
  
 
'''Antibody'''
 
'''Antibody'''
dilute the anitbody 1:10000 (you can freeze the Blotto solution and reuse it)
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*dilute the anitbody 1:10000 (you can freeze the Blotto solution and reuse it)
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'''The reference'''
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<pubmed> 20572937</pubmed>
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==  Return to [[Plasmids]] ==

Latest revision as of 13:58, 3 June 2013

pGP1331: click to enlarge

General comments

Integrative plasmid for the fusion of 3x FLAG tag to the C-terminus of a protein, keeping the control of the expression under its natural promotor

  • E.coli: multicopy plasmid, select for ampicillin
  • B. subtilis: no ori, select for spectinomycin

Hints for the usage

  • amplify the last 600bp of your gene of interest,
  • skip the Stop-codon of the gene in the reverse primer
  • take care that the integration is in-frame
  • Don't use XbaI and KpnI for cloning. They cut the vector twice!

Antibody

  • dilute the anitbody 1:10000 (you can freeze the Blotto solution and reuse it)

The reference

Return to Plasmids