Purpose(Empty Backbone) FX cloning Saccharomyces cerevisiae expression vector with GAL1 promoter and N-terminal 10x His tag and 3C protease cleavage site
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||49024||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
- Backbone size (bp) 7638
Modifications to backbonemodified for compatibility with FX cloning and added tags/fusion proteins
Vector typeYeast Expression
- Promoter GAL1
/ Fusion Proteins
- decaHis (10x His) (N terminal on backbone)
- 3C protease site (PreScission site) (N terminal on backbone)
Growth in Bacteria
Bacterial Resistance(s)Chloramphenicol and Ampicillin
Copy numberLow Copy
- Cloning method Unknown
- 5′ sequencing primer GAL1
- 3′ sequencing primer CYC1 (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
Constructed by Dr. Stephan Schenck, Dutzler lab, Dept of Biochemistry, University of Zurich, Switzerland.
The ampicillin resistance cassette is located at bp# 3637-4497.
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:pYEXNH3 was a gift from Raimund Dutzler & Eric Geertsma (Addgene plasmid # 49024 ; http://n2t.net/addgene:49024 ; RRID:Addgene_49024)
For your References section:A versatile and efficient high-throughput cloning tool for structural biology. Geertsma ER, Dutzler R. Biochemistry. 2011 Apr 19;50(15):3272-8. Epub 2011 Mar 25. 10.1021/bi200178z PubMed 21410291