pIVT-A3A-DEN2
(Plasmid
#238019)
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Purposefor DNA-free cytosine base editing in rice and wheat or other plants
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 238019 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 |
Backbone
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Vector backbonepnCas9-PBE
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Backbone manufacturerCaixia Gao, Addgene Plasmid #98164
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Vector typePlant 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)XL10 Gold
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Growth instructionsWhile the plasmid can be maintained in DH5alpha, please note that the polyA sequence on the plasmid may experience partial adenine (A) loss during E. coli amplification. Therefore, it's essential to pick single colonies for sequencing verification after expansion. The depositing lab specifically selected the XL10 strain because it demonstrates relatively less polyA sequence loss compared to other strains.
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameA3A-nSpCas9(D10A)-UGI
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SpeciesOther
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MutationD10A for SpCas9
- Promoter T7
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.
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:
pIVT-A3A-DEN2 was a gift from Caixia Gao (Addgene plasmid # 238019 ; http://n2t.net/addgene:238019 ; RRID:Addgene_238019) -
For your References section:
An efficient mRNA delivery system for genome editing in plants. Qiu F, Xue C, Liu J, Li B, Gao Q, Liang R, Chen K, Gao C. Plant Biotechnol J. 2025 Apr;23(4):1348-1358. doi: 10.1111/pbi.14591. Epub 2025 Feb 10. 10.1111/pbi.14591 PubMed 39928528