pEIAV-iSyn-eGFPW
(Plasmid
#80161)
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PurposeExpression in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 80161 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneEIAV
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Backbone manufacturerJohn Olsen UNC
- Backbone size w/o insert (bp) 4876
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Vector typeLentiviral
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 numberHigh Copy
Gene/Insert
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Gene/Insert nameeGFP
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SpeciesAequorea victoria
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Insert Size (bp)720
- Promoter iSyn
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site KpnI (not destroyed)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer hSyn1pro-F
- 3′ sequencing primer WPRE-R (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made bybackbone from John Olsen UNC
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:
pEIAV-iSyn-eGFPW was a gift from Edward Callaway (Addgene plasmid # 80161 ; http://n2t.net/addgene:80161 ; RRID:Addgene_80161) -
For your References section:
Optical control of retrogradely infected neurons using drug-regulated "TLoop" lentiviral vectors. Cetin A, Callaway EM. J Neurophysiol. 2014 May;111(10):2150-9. doi: 10.1152/jn.00495.2013. Epub 2014 Feb 26. 10.1152/jn.00495.2013 PubMed 24572099