PurposeVector to create a cassette for homologous recombination in S. cerevisiae; adds a C-terminal tDimer2 Strep-tag II followed by HIS5 selection marker
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||63789||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
Backbone manufacturerMark A. Sheff and Kurt S. Thorn
- Backbone size w/o insert (bp) 5416
- Total vector size (bp) 5456
Vector typeE. coli cloning vector
Growth in Bacteria
Bacterial Resistance(s)Ampicillin, 100 μg/mL
Copy numberHigh Copy
Gene/Insert nametDimer2-Strep-tag II followed by HIS5
- Promoter none
/ Fusion Protein
- tDimer2-Strep-tag II (C terminal on backbone)
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site KpnI (not destroyed)
- 5′ sequencing primer pQE_for
- 3′ sequencing primer pQE_rev (Common Sequencing Primers)
A portion of this plasmid was derived from a plasmid made byMark A. Sheff and Kurt S. Thorn (pKT146)
Terms and Licenses
- Not Available to Industry
- Zeocin® is an InvivoGen trademark.
The Strep-tag II sequence is adapted from the sequence of commercial Strep-tag II plasmids offered by IBA, Goettingen, Germany.
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:pGS1613 was a gift from Monika Golas & Bjoern Sander (Addgene plasmid # 63789 ; http://n2t.net/addgene:63789 ; RRID:Addgene_63789)
For your References section:Strep-tag II and Twin-Strep Based Cassettes for Protein Tagging by Homologous Recombination and Characterization of Endogenous Macromolecular Assemblies in Saccharomyces cerevisiae. Rai J, Pemmasani JK, Voronovsky A, Jensen IS, Manavalan A, Nyengaard JR, Golas MM, Sander B. Mol Biotechnol. 2014 Jun 27. 10.1007/s12033-014-9778-5 PubMed 24969434