MultiMate 5 colors
(Plasmid
#206266)
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PurposeExpression of 5 fluorescently labelled proteins in mammalian cells. Can be used as a CRE-donor (MultiBac system)
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 206266 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMMACE DEST CMV H2B IRFP713
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Vector typeMammalian Expression ; Recombinant baculovirus production, CRE Acceptor (MultiBac)
Growth in Bacteria
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Bacterial Resistance(s)Gentamicin, 10 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameH2B (H. Sapiens), Actin and Tubulin (B. taurus), mito mCherry (Synthetic), CyOFP1 (E. quadricolor)
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SpeciesOther
Cloning Information
- Cloning method Gateway Cloning
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made byH2B-iRFP was PCR amplified from pCAG-H2BtdiRFP-IP (Addgene plasmid #47884, Miyanari Y. et al. Nat Struct Mol Biol. 2013)EYFP-Tubulin and mTFP1-Actin were amplified from 5-colours MultiBac vectors (Mansouri et al. Nat Comm 2016)Mito-mCherry was generated by fusing mCherry from 7TGC (Addgene plasmid#24304) to the COX8 mitochondrial targeting sequence from 5-colours MultiBac vectors (Mansouri et al. 2016)CyOFP1 (Chu et al. Nat Biotechnology 2016)fused to the endoplasmic reticulum targeting sequence (ER) was synthesised by Twist Bioscience
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:
MultiMate 5 colors was a gift from Imre Berger (Addgene plasmid # 206266 ; http://n2t.net/addgene:206266 ; RRID:Addgene_206266) -
For your References section:
Highly efficient CRISPR-mediated large DNA docking and multiplexed prime editing using a single baculovirus. Aulicino F, Pelosse M, Toelzer C, Capin J, Ilegems E, Meysami P, Rollarson R, Berggren PO, Dillingham MS, Schaffitzel C, Saleem MA, Welsh GI, Berger I. Nucleic Acids Res. 2022 Jul 22;50(13):7783-7799. doi: 10.1093/nar/gkac587. 10.1093/nar/gkac587 PubMed 35801912