PB-PE iSM_PPL2
(Plasmid
#235996)
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PurposeExpresses iSM_PPL2 prime editor and pegRNA in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 235996 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 |
Backbone
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Vector backbonePB-PE
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Backbone manufacturerDr. Reto Eggenschwiler
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Vector typeMammalian Expression, CRISPR, Synthetic Biology ; piggyBac transposon
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature30°C
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Growth Strain(s)NEB Stable
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameiSM_PPL2_H840A-PE2-MMLV-RT(dBB)-P2A-PAC_dTK(dBB)
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Alt nameiSM_PPL2 prime editor
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SpeciesSynthetic
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Mutationreplacement of 5 amino acids of Smac-Cas9 PL2 with 16 amino acids from Spy-Cas9 PL2
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Tags
/ Fusion Proteins
- bpSV40 NLS (N terminal on insert)
- bpSV40 NLS (C terminal on insert)
Resource Information
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Supplemental Documents
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
Can be integrated into genome using hyPBase. Contains both, prime editor and U6 promoter driven site for insertion of pegRNA. Can be employed for transient expression experiments, but in case pegRNA is added on a separate plasmid, removal of U6 in PB-PE vector is recommended.
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:
PB-PE iSM_PPL2 was a gift from Tobias Cantz (Addgene plasmid # 235996 ; http://n2t.net/addgene:235996 ; RRID:Addgene_235996) -
For your References section:
PAM-interacting domain turn-helix 51 motifs can improve Cas9-SpRY activity. Eggenschwiler R, Hoffmann T, Dmytrenko O, Opitz M, Ackel-Zakour M, Wang P, McCallan SA, Fraguas-Eggenschwiler M, Niemann H, Patronov A, Beisel CL, Cantz T. Nucleic Acids Res. 2025 Aug 11;53(15):gkaf782. doi: 10.1093/nar/gkaf782. 10.1093/nar/gkaf782 PubMed 40808297