pCAG_N-SplitLuc-PP7
(Plasmid
#261209)
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PurposeN-SplitLuc part of firefly luciferase to be used as cargo in RNA transfer vehicles
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Depositing Lab
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Depositing OrganizationHelmholtz Munich
Located in Germany -
Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 261209 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
Backbone
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Vector backbonepCAG
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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 numberHigh Copy
Gene/Insert
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Gene/Insert nameN-FlucV2-N-gp41-N5coil-PEST-PP7
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Insert Size (bp)1764
- Promoter CAG
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site PacI (unknown if destroyed)
- 3′ cloning site SacI (unknown if destroyed)
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.
Depositor Comments
Please visit https://doi.org/10.21203/rs.3.rs-5123765/v1 for Research Square preprint.
HELMHOLTZ MUNICH has filed a patent (WO2026068725A1) disclosing the capabilities of Material, and retains ownership rights to N-SplitLuc-PP7 Material.
Recipient agrees not to file for any intellectual property protection for Material.
Please note that any use of the Material or the HELMHOLTZ MUNICH Information for any commercial purpose — or by, on behalf of or in collaboration with any for-profit entity — requires a license from HELMHOLTZ MUNICH. To obtain such a license, please contact HELMHOLTZ MUNICH by directing your request to: [email protected].
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:
pCAG_N-SplitLuc-PP7 was a gift from Wolfgang Wurst (Addgene plasmid # 261209 ; http://n2t.net/addgene:261209 ; RRID:Addgene_261209) -
For your References section:
Creating bottom-up RNA transfer vehicles from synthetic protein assemblies. Schuhmacher MK, Gruber C, Lang CMR, Ruijpers RMW, Mazneykova L, Beinsteiner B, Krus A, Tremmel B, Reinhardt F, Kadletz K, Ma Z, Casalta L, Cambra Bort JM, Otify DY, Balken I, Hetzel L, Merl-Pham J, Dorn T, Luchner M, Bauersachs L, Ganea K, Wieser N, Emrich A, Yagmur E, Rager K, Sagindykova G, Armbrust N, Geilenkeuser J, Westmeyer GG, Becirovic E, Biel M, Istvanffy R, Vogt Weisenhorn DM, Truong DJ, Theis FJ, Ebert G, Moretti A, Erturk A, Bahr A, Kupatt C, Jasnin M, Klymiuk N, Giesert F, Wurst W. Nature. 2026 Sep 2. doi: 10.1038/s41586-026-10952-3. 10.1038/s41586-026-10952-3 PubMed 42686908