pICE-HA-CtIP-siR-N289A-H290A
(Plasmid
#82032)
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PurposePlasmid for constitutive or doxy-inducible expression of N289A+H290A mutant of human CtIP resistant to a siRNA. Confers resistance to puromycin. Use T-REx cells for doxycycline-inducible expression.
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Depositing Labs
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 82032 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepICE
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Backbone manufacturerSynthetic - Addgene plasmid #46960
- Backbone size w/o insert (bp) 5011
- Total vector size (bp) 7705
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Modifications to backboneHA tag and cloning sites
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Vector typeMammalian Expression
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Selectable markersPuromycin
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 nameCtIP
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Alt nameRBBP8
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Alt namehSae2
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SpeciesH. sapiens (human)
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Insert Size (bp)2752
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MutationEndonuclease-dead mutant: N289A+H290A CtIP; Mutations making the cDNA resistant to a siRNA
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Entrez GeneRBBP8 (a.k.a. COM1, CTIP, JAWAD, JWDS, RIM, SAE2, SCKL2)
- Promoter CMV-tet
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Tag
/ Fusion Protein
- HA (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site MluI (not destroyed)
- 5′ sequencing primer CMV-F
- 3′ sequencing primer BGH-R (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.
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:
pICE-HA-CtIP-siR-N289A-H290A was a gift from Sébastien Britton & Patrick Calsou (Addgene plasmid # 82032 ; http://n2t.net/addgene:82032 ; RRID:Addgene_82032) -
For your References section:
Coordinated nuclease activities counteract Ku at single-ended DNA double-strand breaks. Chanut P, Britton S, Coates J, Jackson SP, Calsou P. Nat Commun. 2016 Sep 19;7:12889. doi: 10.1038/ncomms12889. 10.1038/ncomms12889 PubMed 27641979