pN3FS-CYC1
(Plasmid
#85783)
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PurposeN-ICE plasmid pH3FS-CYC1
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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 | 85783 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUG6
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Backbone manufacturerEuroscarf
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Vector typeYeast Expression, Cre/Lox
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Selectable markersNourseothricin Sulfate
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 numberHigh Copy
Gene/Insert
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Gene/Insert nameloxP-NatMX-loxP-CYC1p-3FLAG
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SpeciesS. cerevisiae (budding yeast), Synthetic
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Mutation*(see below)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NotI (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer T7 promoter
- 3′ sequencing primer CGCGTCAGCGGGTGTTGG (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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
*Note: Addgene's quality control sequencing finds a P77L amino acid residue substitution in the Nourseothricin resistance gene, but this residue change is not thought to affect antibiotic selection.
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:
pN3FS-CYC1 was a gift from Scott Briggs (Addgene plasmid # 85783 ; http://n2t.net/addgene:85783 ; RRID:Addgene_85783) -
For your References section:
N-ICE plasmids for generating N-terminal 3 x FLAG tagged genes that allow Inducible, Constitutive, or Endogenous expression in Saccharomyces cerevisiae. Zhang Y, Serratore ND, Briggs SD. Yeast. 2016 Dec 12. doi: 10.1002/yea.3226. 10.1002/yea.3226 PubMed 27943405