|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||8730||Standard format: Plasmid sent in bacteria as agar stab||1||$85|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 4900
Vector typeYeast Expression
Selectable markersURA3 ; C. albicans
Growth in Bacteria
Bacterial Resistance(s)Ampicillin, 100 μg/mL
Alt nameCodon-optimized GFP variant
Alt namepKT209 (pFA6a–link–yEGFP–CaURA3)
/ Fusion Protein
- Codon optimized linker (N terminal on backbone)
- Cloning method Restriction Enzyme
- 5′ cloning site PacI (not destroyed)
- 3′ cloning site AscI (not destroyed)
- 5′ sequencing primer SP6 (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
- Zeocin® is an InvivoGen trademark.
Full name of this plasmid is pFA6a-link-yEGFP-CaURA3. An codon-optimized linker was added into the yEGFP to improve expression level. C. albicans URA3 (CaURA3) was introduced by subcloning the BglII/SacI fragment of pAG60 (Goldstein et al., 1999) into the plasmid, in place of SpHIS5.
The yeast GFP used to create this plasmid contained a point mutation M233I that is present in all GFP variants derived from this original yEGFP. The mutation had no effect on fluorescence (see associated publication for more details).
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:pKT0209 was a gift from Kurt Thorn (Addgene plasmid # 8730 ; http://n2t.net/addgene:8730 ; RRID:Addgene_8730)
For your References section:Optimized cassettes for fluorescent protein tagging in Saccharomyces cerevisiae. Sheff MA, Thorn KS. Yeast 2004 Jun;21(8):661-70. 10.1002/yea.1130 PubMed 15197731