pAAV-Syn-Mac-GFP
(Plasmid
#58853)
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PurposeAAV-mediated expression of Mac-GFP under the Syn promoter
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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 | 58853 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
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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 backboneAAV
- Backbone size w/o insert (bp) 4708
- Total vector size (bp) 6379
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Vector typeMammalian Expression, AAV
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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Growth instructionsStbl3 at 30C (use carbenicillin if using Stbl3) OR DH5a at 37C
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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameMac-GFP
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Alt nameLeptosphaeria maculans opsin
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SpeciesLeptosphaeria maculans
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Insert Size (bp)1671
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GenBank IDGU045595.1
- Promoter Syn
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Tag
/ Fusion Protein
- GFP (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer CTGCGTATGAGTGCAAG
- 3′ sequencing primer cagcgtatccacatagcg (Common Sequencing Primers)
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
Plasmid is completely sequenced by the depositing lab except parts of the origin and both ITRs. Multiple digestions were done to verify the vector structure. The construct and the virus were both tested in vitro.
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-Syn-Mac-GFP was a gift from Edward Boyden (Addgene plasmid # 58853 ; http://n2t.net/addgene:58853 ; RRID:Addgene_58853) -
For your References section:
High-performance genetically targetable optical neural silencing by light-driven proton pumps. Chow BY, Han X, Dobry AS, Qian X, Chuong AS, Li M, Henninger MA, Belfort GM, Lin Y, Monahan PE, Boyden ES. Nature. 2010 Jan 7. 463(7277):98-102. 10.1038/nature08652 PubMed 20054397