M4758 KanMX::URA3 Disruptor Converter
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||51688||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
Vector backboneM4757 (kanMX::TRP1), Addgene plasmid #51687
Vector typeYeast Expression ; yeast marker swap
Growth in Bacteria
SpeciesS. cerevisiae (budding yeast)
Entrez GeneURA3 (a.k.a. YEL021W)
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site XhoI (destroyed during cloning)
- 5′ sequencing primer SP6
- 3′ sequencing primer T7 (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
M4758 (kanMX::URA3) was made by digesting M4757 with BamHI and SalI and inserting a 1.2 kb BamHI–XhoI fragment with URA3 from plasmid M522.
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:M4758 KanMX::URA3 Disruptor Converter was a gift from David Stillman (Addgene plasmid # 51688 ; http://n2t.net/addgene:51688 ; RRID:Addgene_51688)
For your References section:New 'marker swap' plasmids for converting selectable markers on budding yeast gene disruptions and plasmids. Voth WP, Jiang YW, Stillman DJ. Yeast. 2003 Aug;20(11):985-93. 10.1002/yea.1018 PubMed 12898713