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PurposeI-SceI endonuclease expression vector with mammalian promoter to introduce a DSB at a genomic I-SceI site
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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 | 26477 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCAGGS
- Backbone size w/o insert (bp) 3073
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Vector typeMammalian Expression
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 namepCBASceI
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Alt nameCBAS
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Insert Size (bp)2583
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Tag
/ Fusion Protein
- HA (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site XhoI (destroyed during cloning)
- 3′ cloning site XhoI (destroyed during cloning)
- 5′ sequencing primer n/a (Common Sequencing Primers)
Resource Information
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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:
pCBASceI was a gift from Maria Jasin (Addgene plasmid # 26477 ; http://n2t.net/addgene:26477 ; RRID:Addgene_26477) -
For your References section:
Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations. Richardson C, Moynahan ME, Jasin M. Genes Dev. 1998 Dec 15. 12(24):3831-42. 10.1101/gad.12.24.3831 PubMed 9869637