pMB952:PB-CAG-PuroR-nGFP-FLEx-SaCas9-P2A-mCherry-WPRE
(Plasmid
#168107)
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PurposePiggyBac transposon vector constitutively driving PuroR-eGFP and conditionally expressing S.aureus Cas9 and mCherry
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 168107 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonePBCAG-eGFP
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Backbone manufacturerAddgene #40973
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Vector typeCre/Lox, CRISPR
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Selectable markersPuromycin ; eGFP
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)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameCas9-P2A-mCherry
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Alt nameSaCas9-P2A-mCherry
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SpeciesS.aureus
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Insert Size (bp)4122
- Promoter CAG
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Tag
/ Fusion Protein
- HA (C terminal on insert)
Cloning Information
- Cloning method Gibson Cloning
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
Puromycin selection disappears following Cre recombination.
Please visit https://www.biorxiv.org/content/10.1101/2021.05.27.445896v1 for BioRxiv preprint.
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:
pMB952:PB-CAG-PuroR-nGFP-FLEx-SaCas9-P2A-mCherry-WPRE was a gift from Erich Jarvis (Addgene plasmid # 168107 ; http://n2t.net/addgene:168107 ; RRID:Addgene_168107) -
For your References section:
Induction of an immortalized songbird cell line allows for gene characterization and knockout by CRISPR-Cas9. Biegler MT, Fedrigo O, Collier P, Mountcastle J, Haase B, Tilgner HU, Jarvis ED. Sci Rep. 2022 Mar 14;12(1):4369. doi: 10.1038/s41598-022-07434-7. 10.1038/s41598-022-07434-7 PubMed 35288582