pSI-218
(Plasmid
#197139)
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Purpose(Empty Backbone) All-in-vector of SpCas9 gRNA cloning sites (BsmBI) and CMVp-Target-AID expression unit
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 197139 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA3.1
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Backbone manufacturerInvitrogen
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Vector typeMammalian Expression, CRISPR
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Selectable markersNeomycin (select with G418)
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Tag
/ Fusion Protein
- SpCas9-PmCDA1-UGI (N terminal on insert)
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 numberHigh Copy
Gene/Insert
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Gene/Insert nameNone
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MutationSpCas9(D10A)
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Tag
/ Fusion Protein
- SpCas9-PmCDA1-UGI (N 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
https://benchling.com/s/seq-ir6EdyAiwwADqkZoUTvT?m=slm-OO1VK36RD5vy05CbCzFP
Please visit https://www.biorxiv.org/content/10.1101/2023.01.18.524633v1 for bioRxiv preprint. This plasmid is relatively unstable due to repetitive sequences and other genetic element cloned from retrovirus. Please be sure to use NEB stable cells and incubate at 30C.
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:
pSI-218 was a gift from Nozomu Yachie (Addgene plasmid # 197139 ; http://n2t.net/addgene:197139 ; RRID:Addgene_197139) -
For your References section:
A multi-kingdom genetic barcoding system for precise target clone isolation. Ishiguro S, Ishida K, Sakata RC, Mori H, Takana M, King S, Bashth O, Ichiraku M, Masuyama N, Takimoto R, Kijima Y, Adel A, Toyoshima H, Seki M, Oh JH, Archambault AS, Nishida K, Kondo A, Kuhara S, Aburatani H, Klein Geltink RI, Takashima Y, Shakiba N, Yachie N. bioRxiv 2023.01.18.524633 10.1101/2023.01.18.524633