pLenti NLuc398-G8NCRD IRES G8NCRD-CLuc394
(Plasmid
#128386)
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PurposeExpresses a split firefly luciferase reporter based on the N terminal carbohydrate recognition domain of human galectin 8, which concentrates inside endosomes following endosomal disruption
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 128386 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepLV
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Backbone manufacturerVectorBuilder
- Backbone size w/o insert (bp) 9096
- Total vector size (bp) 12473
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Modifications to backboneEF1A promoter; EGFP:T2A:Bsd selection
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Vector typeMammalian Expression, Lentiviral, Luciferase, Synthetic Biology
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Selectable markersBlasticidin ; EGFP
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 numberUnknown
Gene/Insert 1
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Gene/Insert nameNLuc-3xGGGGS-Gal8-NCRD
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Alt nameLuc2
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SpeciesH. sapiens (human), Synthetic
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Insert Size (bp)1716
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MutationN terminal carbohydrate recognition domain fused to N terminal Luc fragment
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Entrez GeneLGALS8 (a.k.a. Gal-8, PCTA-1, PCTA1, Po66-CBP)
- Promoter EF1A
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Tag
/ Fusion Protein
- N-terminal luc2 fragment (N terminal on insert)
Cloning Information for Gene/Insert 1
- Cloning method Unknown
- 5′ sequencing primer none (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameGal8-NCRD-3xGGGGS-CLuc398
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SpeciesH. sapiens (human)
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Insert Size (bp)990
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MutationN terminal carbohydrate recognition domain fused to C terminal Luc fragment
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Entrez GeneLGALS8 (a.k.a. Gal-8, PCTA-1, PCTA1, Po66-CBP)
- Promoter IRES
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Tag
/ Fusion Protein
- C-terminal luc2 fragment (C terminal on insert)
Cloning Information for Gene/Insert 2
- Cloning method Unknown
- 5′ sequencing primer none (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byOutsourced synthesis
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:
pLenti NLuc398-G8NCRD IRES G8NCRD-CLuc394 was a gift from Craig Duvall (Addgene plasmid # 128386 ; http://n2t.net/addgene:128386 ; RRID:Addgene_128386) -
For your References section:
Genetically encoded split-luciferase biosensors to measure endosome disruption rapidly in live cells. Kilchrist KV, Tierney JW, Duvall CL. ACS Sens. 2020 Jun 23. doi: 10.1021/acssensors.0c00103. 10.1021/acssensors.0c00103 PubMed 32573202