|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||35452||Standard format: Plasmid sent in bacteria as agar stab||1||$85|
This material is available to academics and nonprofits only.
- Backbone size (bp) 4787
Vector typeYeast centromere vector
- Promoter None
Growth in Bacteria
Bacterial Resistance(s)Ampicillin, 100 μg/mL
Copy numberHigh Copy
- Cloning method Restriction Enzyme
- 5′ sequencing primer M13 Forward, T7
- 3′ sequencing primer M13 Reverse (Common Sequencing Primers)
A portion of this plasmid was derived from a plasmid made byDaniel J. Lew, Duke University Medical Center Chandra Tucker, Duke University (now at University of Colorado, Boulder)
Terms and Licenses
- Not Available to Industry
- Zeocin® is an InvivoGen trademark.
TRP1 has been modified to remove HindIII and XbaI sites without altering the amino acid sequence of the Trp1 protein.
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:pRSII414 was a gift from Steven Haase (Addgene plasmid # 35452 ; http://n2t.net/addgene:35452 ; RRID:Addgene_35452)
For your References section:New and Redesigned pRS Plasmid Shuttle Vectors for Genetic Manipulation of Saccharomycescerevisiae. Chee MK, Haase SB. G3 (Bethesda). 2012 May;2(5):515-26. Epub 2012 May 1. 10.1534/g3.111.001917 PubMed 22670222