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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 13534 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepRSET-B
- Backbone size w/o insert (bp) 2897
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Vector typeBacterial Expression
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
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Gene/Insert nameFLIPW-CTYT
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Alt nameECFP-TrpR-Venus-TrpR
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Alt nameTrpR
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SpeciesE. coli
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Insert Size (bp)2200
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Tags
/ Fusion Proteins
- See map
- See map
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer N/A (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byVenus is from Dr. Atsushi Miyawaki.
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Article Citing this Plasmid
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.
Depositor Comments
For more information, see
http://carnegiedpb.stanford.edu/research/frommer/nanosensors/index.html
1st TrpR was gateway cloned into FLIP cassette. 2nd TrpR is cloned into EcoRI.
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:
pTK204 was a gift from Wolf Frommer (Addgene plasmid # 13534 ; http://n2t.net/addgene:13534 ; RRID:Addgene_13534) -
For your References section:
Nanosensor detection of an immunoregulatory tryptophan influx/kynurenine efflux cycle. Kaper T, Looger LL, Takanaga H, Platten M, Steinman L, Frommer WB. PLoS Biol. 2007 Oct;5(10):e257. 10.1371/journal.pbio.0050257 PubMed 17896864