pcDNA3.1 T21R-vhhGFP4-T2A-mCherry
(Plasmid
#225587)
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PurposeMammalian expression vector for TRIM21 RING-vhhGFP4 anti-GFP degrader with a self-cleaving T2A-mCherry fluorescent expression reporter
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Depositing Lab
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Sequence Information
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Sequences (1) — Accept Affinity Reagent Sequence Policy
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Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 225587 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA3.1
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Vector typeMammalian Expression
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)DH5alpha
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameT21R-vhhGFP4-T2A-mCherry
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SpeciesSynthetic
- Promoter CMV
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Tag
/ Fusion Protein
- mCherry (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site XbaI (not destroyed)
- 5′ sequencing primer N/A (Common Sequencing Primers)
Resource Information
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:
pcDNA3.1 T21R-vhhGFP4-T2A-mCherry was a gift from William McEwan (Addgene plasmid # 225587 ; http://n2t.net/addgene:225587 ; RRID:Addgene_225587) -
For your References section:
Aggregate-selective removal of pathological tau by clustering-activated degraders. Benn J, Cheng S, Keeling S, Smith AE, Vaysburd MJ, Boken D, Miller LVC, Katsinelos T, Franco C, Dupre E, Danis C, Landrieu I, Buee L, Klenerman D, James LC, McEwan WA. Science. 2024 Aug 30;385(6712):1009-1016. doi: 10.1126/science.adp5186. Epub 2024 Aug 29. 10.1126/science.adp5186 PubMed 39208111