MultiMate-Rainbow
(Plasmid
#206252)
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PurposeExpression of 7 fluorescently labelled proteins in mammalian cells. Can be used to generate recombinant baculovirus particles.
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Depositing Lab
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Depositing OrganizationUniversity of Bristol
Located in United Kingdom of Great Britain and Northern Ireland -
Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 206252 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
| DNA | 206252-D50 | 50 μg of DNA in Tris buffer | $495 | ||
| DNA | 206252-D100 | 100 μg of DNA in Tris buffer | $585 | ||
Backbone
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Vector backbonepMMACE DEST CMV H2B IRFP713
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Vector typeMammalian Expression ; Recombinant baculovirus production (Bac-to-Bac)
Growth in Bacteria
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Bacterial Resistance(s)Gentamicin and Spectinomycin
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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 (human); Actin, Tubulin (B. taurus); mito mCherry, GST mTagBFP1 (Synthetic); CyOFP1 (E. quadricolor); Ctnnb1 (mouse)
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SpeciesOther
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Tag
/ Fusion Protein
- iRFP713 (C terminal on insert)
Cloning Information
- Cloning method Gateway Cloning
Resource Information
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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.mAG beta-catenin was obtained through Gibson assembly of PCR amplified mAG from pL-EF1a mAG-hGeminin (De Jaime-Soguero A. et al. Plos Genetics 2017), and beta-catenin from pL-EF1a beta-catenin SV40 Puro (Aulicino et al. Stem Cell Reports, 2020)
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.
DNA (Catalog # 206252-D50)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 50 μg
- Concentration 1 μg/μL
- Pricing $495 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
DNA (Catalog # 206252-D100)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 100 μg
- Concentration 1 μg/μL
- Pricing $585 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
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-Rainbow was a gift from Imre Berger (Addgene plasmid # 206252 ; http://n2t.net/addgene:206252 ; RRID:Addgene_206252) -
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