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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 | 8729 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepFA6a-link
- Backbone size w/o insert (bp) 4738
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Vector typeYeast Expression
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Selectable markersS. pombe HIS5
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 nameyEGFP
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Alt nameCodon-optimized GFP variant
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Alt namepKT128 (pFA6a–link–yEGFP–SpHIS5)
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Tag
/ Fusion Protein
- Codon optimized linker (N terminal on backbone)
Cloning Information
- 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
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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
Full name of this plasmid is pFA6a-link-yEGFP-SpHIS5. An codon-optimized linker was added into the yEGFP to improve expression level. The selectable marker, Sz. pombe HIS5 (SpHIS5), complements S. cerevisiae HIS3.
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.
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For your Materials & Methods section:
pKT0128 was a gift from Kurt Thorn (Addgene plasmid # 8729 ; http://n2t.net/addgene:8729 ; RRID:Addgene_8729) -
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