PASTA-3_pUC19_HDR-Pa01-attG_TRAC_for-Cas12a
(Plasmid
#247039)
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PurposeEncodes HDR-template for Cas12a-mediated Knock-In of size-reduced Pa01-attG (landing pad) into TRAC gene (exon1). Template region to be PCR-amplified.
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Depositing Lab
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Depositing OrganizationCharite Universitaetsmedizin Berlin
Located in Germany -
Publication
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 247039 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
Backbone
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Vector backbonepUC19
- Backbone size w/o insert (bp) 2686
- Total vector size (bp) 3335
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 namePa01 bacterial attachment site (attB) = genomic attachment site (attG), flanked by human TRAC homology arms
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SpeciesH. sapiens (human); Pseudomonas aeruginosa
Resource Information
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
This HDR-template encoding plasmid can be used together with ePa01 mRNA, which can be generated by IVT from our Addgene plasmid #247041 ('PASTA-5_pUC19_IVT-ePa01'). It enables targeted, (e)Pa01-mediated insertion of our integration-plasmid ‘PASTA-4_pUC19_INT-Pa01-attV_P2A_CD19CAR_bGH-pA’ (Addgene plasmid #247040, provided alongside) into the human TRAC gene. Please visit https://doi.org/10.1101/2025.09.10.675267 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:
PASTA-3_pUC19_HDR-Pa01-attG_TRAC_for-Cas12a was a gift from Dimitrios Wagner (Addgene plasmid # 247039 ; http://n2t.net/addgene:247039 ; RRID:Addgene_247039) -
For your References section:
Versatile and efficient non-viral integration of large transgenes in human T cells via CRISPR knock-in and engineered integrases. Kassing I, Kath J, Nitulescu A-M, Glaser V, Hartmann LM, Pu Y, Huth L, Kārkliņš R, Shaji S, Ringel AR, Pouzolles M, Stein M, Ibrahim DM, Wagner DL. bioRxiv 2025.09.10.675267 10.1101/2025.09.10.675267