pGEX-4T1-14-3-3 epsilon GST
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||13279||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 4969
Vector typeBacterial Expression
Growth in Bacteria
Copy numberHigh Copy
Gene/Insert name14-3-3 epsilon
SpeciesR. norvegicus (rat)
Entrez GeneYwhae (a.k.a. 14-3-3e)
/ Fusion Protein
- GST (N terminal on backbone)
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site SmaI (destroyed during cloning)
- 5′ sequencing primer pGEX (Common Sequencing Primers)
Insert from epsilon-MBP cloned into BamHI and SmaI (which is now lost).
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:pGEX-4T1-14-3-3 epsilon GST was a gift from Michael Yaffe (Addgene plasmid # 13279 ; http://n2t.net/addgene:13279 ; RRID:Addgene_13279)
For your References section:The structural basis for 14-3-3:phosphopeptide binding specificity. Yaffe MB, Rittinger K, Volinia S, Caron PR, Aitken A, Leffers H, Gamblin SJ, Smerdon SJ, Cantley LC. Cell. 1997 Dec 26. 91(7):961-71. 10.1016/S0092-8674(00)80487-0 PubMed 9428519