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PurposeAAV-mediated expression of mEGFP and paAIP2 for optogenetic control of CaMKII
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 91718 | 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
- Backbone size w/o insert (bp) 4650
- Total vector size (bp) 5775
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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)NEB Stable
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Copy numberUnknown
Gene/Insert
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Gene/Insert namemEGFP-P2A-paAIP2
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SpeciesSynthetic
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Insert Size (bp)1239
- Promoter CaMKII 1.3
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site AseI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer gaccccaacgagaagcgcg (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:
CaMKIIP-mEGFP-P2A-paAIP2/pAAV was a gift from Ryohei Yasuda (Addgene plasmid # 91718 ; http://n2t.net/addgene:91718 ; RRID:Addgene_91718) -
For your References section:
Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor. Murakoshi H, Shin ME, Parra-Bueno P, Szatmari EM, Shibata AC, Yasuda R. Neuron. 2017 Apr 5;94(1):37-47.e5. doi: 10.1016/j.neuron.2017.02.036. Epub 2017 Mar 16. 10.1016/j.neuron.2017.02.036 PubMed 28318784