pSIG1
(Plasmid
#226908)
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Purpose(Empty Backbone) MoClo-compatible vectors for dsRNA production in E. coli
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 226908 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepICH47732
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Backbone manufacturerMoClo Toolkit
- Backbone size (bp) 4376
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Modifications to backboneAdd two T7 promoters and terminators, two BsmBI sites, and a negative selection marker, sacB gene.
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Vector typeBacterial Expression, Synthetic Biology
- Promoter T7 promoter
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Selectable markerssacB (select with 10% sucrose)
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
Cloning Information
- Cloning method Golden Gate
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made bySylvestre Marillonnet (Addgene plasmid # 48000).
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
The pSIG plasmids are derived from the level 1 plasmid pICH47732 (addgene #48000) within the MoClo toolkit.
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:
pSIG1 was a gift from Li Hung Chen (Addgene plasmid # 226908 ; http://n2t.net/addgene:226908 ; RRID:Addgene_226908) -
For your References section:
pSIG plasmids, MoClo-compatible vectors for efficient production of chimeric double-stranded RNAs in Escherichia coli HT115 (DE3) strain. Wu C-F, Chang L-P, Lee C, Stergiopoulos I, Chen L-H. Plant Methods 21, 96 (2025). https://doi.org/10.1186/s13007-025-01413-5 10.1186/s13007-025-01413-5