pCAGGS-6015nes
(Plasmid
#108657)
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PurposeA S6 Kinase biosensor based on fluorescence resonance energy transfer (FRET) and those based on bioluminescence energy transfer (BRET)
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 108657 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCAGGS
- Backbone size w/o insert (bp) 4739
- Total vector size (bp) 7939
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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 namehyBRET-S6K-EV
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SpeciesS. cerevisiae (budding yeast), Synthetic; aequorea coerulescens
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Insert Size (bp)3200
- Promoter pCAGGS
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Tag
/ Fusion Protein
- XFP (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site SalI (not destroyed)
- 5′ sequencing primer pCAGGSseq_F
- 3′ sequencing primer pCAGGSseq_R (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.
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:
pCAGGS-6015nes was a gift from Michiyuki Matsuda (Addgene plasmid # 108657 ; http://n2t.net/addgene:108657 ; RRID:Addgene_108657) -
For your References section:
A platform of BRET-FRET hybrid biosensors for optogenetics, chemical screening, and in vivo imaging. Komatsu N, Terai K, Imanishi A, Kamioka Y, Sumiyama K, Jin T, Okada Y, Nagai T, Matsuda M. Sci Rep. 2018 Jun 12;8(1):8984. doi: 10.1038/s41598-018-27174-x. 10.1038/s41598-018-27174-x PubMed 29895862