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PurposeExpresses a nuclear-targeted mCherry control construct, on a CMV reporter
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 58476 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepmCherry-C1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4700
- Total vector size (bp) 4788
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)Top10
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert name3X NLS with 3X stop codons
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SpeciesSV40 virus
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Insert Size (bp)81
- Promoter CMV
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Tag
/ Fusion Protein
- mCherry (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site KpnI (not destroyed)
- 5′ sequencing primer mCherry Forward
- 3′ sequencing primer SV40 polyA Reverse (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made by3X NLS (with stop codons) was cloned by insertion of annealed primers with flanking restriction sites.
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Articles Citing this Plasmid
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:
pmCherry-C1 mCherry-NLS was a gift from Dyche Mullins (Addgene plasmid # 58476 ; http://n2t.net/addgene:58476 ; RRID:Addgene_58476) -
For your References section:
DNA damage induces nuclear actin filament assembly by formin-2 and Spire-1/2 that promotes efficient DNA repair. Belin BJ, Lee T, Mullins RD. Elife. 2015 Aug 19;4. doi: 10.7554/eLife.07735. 10.7554/eLife.07735 PubMed 26287480