|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||45774||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
Modifications to backbonepTacI promoter was removed and replaced by PLtetO-1. Untranslated region was removed and replaced by UTR1, a powerful UTR. Luc gene (firefly Luciferase) was removed and replaced by the fusion protein TetR-deGFP. A transcriptional terminator was added, called T500.
Vector typeBacterial Expression, Synthetic Biology
Growth in Bacteria
Copy numberHigh Copy
Insert Size (bp)1332
- Promoter PLtetO-1
/ Fusion Protein
- Fusion protein of TetR and deGFP, with glycine-serine linker
- Cloning method Unknown
- 5′ sequencing primer GTGAACGTGACGGACGTAAC
- 3′ sequencing primer TCGCCGCACTTATGACTGCGGTATCAGCTCACTCAAAG (Common Sequencing Primers)
A portion of this plasmid was derived from a plasmid made byVincent Noireaux, University of Minnesota
Terms and Licenses
- Not Available to Industry
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:pBEST-PLtetO-1-UTR1-TetR-deGFP-T500 was a gift from Richard Murray (Addgene plasmid # 45774 ; http://n2t.net/addgene:45774 ; RRID:Addgene_45774)