Cherry-ICP0-C3
(Plasmid
#134560)
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PurposeExpresses Cherry-ICP0 fusion protein
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 134560 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepEYFP-C3; vector was modified by substituting mCherry for YFP
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4700
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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)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameICP0
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SpeciesOther
- Promoter CMV
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Tag
/ Fusion Protein
- Cherry (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site blunt XhoI (destroyed during cloning)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer mCherry-F
- 3′ sequencing primer SV40pA-R (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byRoger Everett
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:
Cherry-ICP0-C3 was a gift from Susan Janicki (Addgene plasmid # 134560 ; http://n2t.net/addgene:134560 ; RRID:Addgene_134560) -
For your References section:
Single-cell analysis of Daxx and ATRX-dependent transcriptional repression. Newhart A, Rafalska-Metcalf IU, Yang T, Negorev DG, Janicki SM. J Cell Sci. 2012 Nov 15;125(Pt 22):5489-501. doi: 10.1242/jcs.110148. Epub 2012 Sep 12. 10.1242/jcs.110148 PubMed 22976303