pGS1044
(Plasmid
#63797)
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PurposeVector to create a cassette for homologous recombination in S. cerevisiae; adds a C-terminal 3xFLAG tag and a LEU2 selection marker
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Depositing Labs
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 63797 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUC57
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Backbone manufacturer2710
- Backbone size w/o insert (bp) 2024
- Total vector size (bp) 4686
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Vector typeE. coli cloning vector
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Selectable markersLEU2
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 name3xFLAG followed by KlLEU2
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SpeciesSynthetic
- Promoter none
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Tag
/ Fusion Protein
- 3xFLAG (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site SalI (not destroyed)
- 5′ sequencing primer M13 rev -49 (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byRon Prywes (p3xFLAG-S2P; Addgene #32966); derived from plasmid pGS1034
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.
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:
pGS1044 was a gift from Monika Golas & Bjoern Sander (Addgene plasmid # 63797 ; http://n2t.net/addgene:63797 ; RRID:Addgene_63797) -
For your References section:
Dual tagging as an approach to isolate endogenous chromatin remodeling complexes from Saccharomyces cerevisiae. Lin TY, Voronovsky A, Raabe M, Urlaub H, Sander B, Golas MM. Biochim Biophys Acta. 2015 Mar;1854(3):198-208. doi: 10.1016/j.bbapap.2014.11.009. Epub 2014 Dec 5. 10.1016/j.bbapap.2014.11.009 PubMed 25486077