M4758 KanMX::URA3 Disruptor Converter
(Plasmid
#51688)
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PurposeYeast marker swap plasmid for converting KanMX3 to URA3
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 51688 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneM4757 (kanMX::TRP1), Addgene plasmid #51687
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Vector typeYeast Expression ; yeast marker swap
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Selectable markersURA3
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameURA3
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SpeciesS. cerevisiae (budding yeast)
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Entrez GeneURA3 (a.k.a. YEL021W)
Cloning Information
- 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
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
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.
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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