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PurposeClover-mRuby2 tandem fusion for FRET calibration
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 49089 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA3-Clover (Addgene plasmid #40259)
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Backbone manufacturerMichael Lin
- Backbone size w/o insert (bp) 6127
- Total vector size (bp) 6910
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Modifications to backboneinserted NheI/DraIII fragment containing mRuby2 from Addgene plasmid #40260 into XbaI/DraIII site of Addgene plasmid #40259
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
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 numberLow Copy
Gene/Insert
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Gene/Insert nameClover-mRuby2 fusion
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SpeciesSynthetic; Aequorea victoria
- Promoter CMV
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site XbaI (destroyed during cloning)
- 3′ cloning site DraIII (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer SP6 (Common Sequencing Primers)
Resource Information
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Articles Citing this Plasmid
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-Clover-mRuby2 was a gift from Kurt Beam (Addgene plasmid # 49089 ; http://n2t.net/addgene:49089 ; RRID:Addgene_49089)