|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||13533||Standard format: Plasmid sent in bacteria as agar stab||1||$65|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 2897
Vector typeBacterial Expression
Growth in Bacteria
Copy numberHigh Copy
Insert Size (bp)2000
/ Fusion Proteins
- ECFP (N terminal on insert)
- Venus (C terminal on insert)
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer N/A (Common Sequencing Primers)
A portion of this plasmid was derived from a plasmid made byVenus is from Dr. Atsushi Miyawaki. Please ask Dr. Miyawaki for permission to use Venus in another vector.
Terms and Licenses
For more information, see
TrpR was gateway cloned into FLIP cassette.
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.
For your Materials & Methods section:pTK164 was a gift from Wolf Frommer (Addgene plasmid # 13533 ; http://n2t.net/addgene:13533 ; RRID:Addgene_13533)
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