pTetR-LasR-pLuxR-GFP
(Plasmid
#171159)
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PurposeSensing Device with Reporter protein
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 171159 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepSB1A2
- Backbone size w/o insert (bp) 2079
- Total vector size (bp) 3966
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Vector typeBacterial Expression, Synthetic Biology
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert 1
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Gene/Insert namelasR
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Alt nametranscriptional regulator LasR
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SpeciesPseudomonas aeruginosa
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Insert Size (bp)723
- Promoter pTet
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site XbaI (destroyed during cloning)
- 3′ cloning site SpeI (destroyed during cloning)
- 5′ sequencing primer Nil
- 3′ sequencing primer Nil (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert namegfp
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Alt namegreen fluorescence protein GFP
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SpeciesAequorea victoria
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Insert Size (bp)717
- Promoter pLux
Cloning Information for Gene/Insert 2
- Cloning method Restriction Enzyme
- 5′ cloning site XbaI (destroyed during cloning)
- 3′ cloning site SpeI (destroyed during cloning)
- 5′ sequencing primer Nil
- 3′ sequencing primer Nil (Common Sequencing Primers)
Resource Information
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Supplemental Documents
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
pTetR-LasR-pLuxR-GFP was a gift from Matthew Chang (Addgene plasmid # 171159 ; http://n2t.net/addgene:171159 ; RRID:Addgene_171159) -
For your References section:
Engineering microbes to sense and eradicate Pseudomonas aeruginosa, a human pathogen. Saeidi N, Wong CK, Lo TM, Nguyen HX, Ling H, Leong SS, Poh CL, Chang MW. Mol Syst Biol. 2011 Aug 16;7:521. doi: 10.1038/msb.2011.55. 10.1038/msb.2011.55 PubMed 21847113