pAAV-CAG-eGFP-Tag100
(Plasmid
#242779)
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PurposeAAV transfer plasmid expressing eGFP-Tag100 under a CAG 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) | |
|---|---|---|---|---|---|
| Plasmid | 242779 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 | |
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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 + $32 USD for plasmid.
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Backbone
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Vector backbonepAAV-CAG-GFP (Addgene Plasmid 37825)
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Backbone manufacturerEdward Boyden
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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 Temperature30°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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SpeciesSynthetic
- Promoter CAG
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Tag
/ Fusion Protein
- Tag100 (C terminal on insert)
Cloning Information
- Cloning method Gibson Cloning
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.
Depositor Comments
Please visit https://doi.org/10.1101/2025.09.26.678648 for bioRxiv preprint.
There is a minor discrepancy between the Addgene NGS sequence and the depositor sequence: 1bp indel in R-ITR. Depositor confirms this is not of concern for plasmid 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-CAG-eGFP-Tag100 was a gift from Andrew Payne (Addgene plasmid # 242779 ; http://n2t.net/addgene:242779 ; RRID:Addgene_242779) -
For your References section:
Combinatorial protein barcodes enable self-correcting neuron tracing with nanoscale molecular context. Park SY, Sheridan A, An B, Jarvis E, Lyudchik J, Patton W, Axup JY, Chan SW, Damstra HGJ, Leible D, Leung KS, Magno CA, Meeran A, Michalska JM, Rieger F, Wang C, Wu M, Church GM, Funke J, Huffman T, Leeper KGC, Truckenbrodt S, Winnubst J, Kornfeld JMR, Boyden ES, Rodriques SG, Payne AC. bioRxiv 2025.09.26.678648 10.1101/2025.09.26.678648