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Purpose(Empty Backbone) Cloning plasmid for the generation of Knock-In in human cells using rAAV.
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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 | 46954 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
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SerotypeSelect serotype for details See details about
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PricingSelect serotype and quantity $ USD for preparation of µL virus + $30 USD for plasmid.
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Backbone
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Vector backbonepAAV-MCS
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Backbone manufacturerAgilent Technologies
- Backbone size (bp) 4650
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Modifications to backboneA 1,345-bp fragment of Ku80 cDNA was digested with NotI–Bsp12OIand cloned as a linker flanked by restrictions sites into NotI-digested pAAV-MCS.
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Vector typeAAV
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)XL1 Blue
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Copy numberHigh Copy
Cloning Information
- Cloning method Restriction Enzyme
Resource Information
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Supplemental Documents
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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.
Depositor Comments
Please note that the Addgene verified sequence found an 11bp deletion in one ITR and D158G in the Ku80 sequence. The depositor confirmed that this does not impact function.
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:
pAAV-MCS2 was a gift from Steve Jackson (Addgene plasmid # 46954 ; http://n2t.net/addgene:46954 ; RRID:Addgene_46954) -
For your References section:
A new method for high-resolution imaging of Ku foci to decipher mechanisms of DNA double-strand break repair. Britton S, Coates J, Jackson SP. J Cell Biol. 2013 Jul 29. 10.1083/jcb.201303073 PubMed 23897892