pBEST-PT7extended-MGapt-UTR1-deGFP
(Plasmid
#227646)
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PurposepT7-driven expression of MGapt and deGFP for quantifying cell-free RNA and protein synthesis with extended T7 promoter.
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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 | 227646 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBEST
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Vector typeSynthetic Biology
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)MG1655-Z1
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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameMG aptamer (MGapt) and deGFP
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SpeciesSynthetic
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
Please visit https://doi.org/10.1101/2023.03.22.533877 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:
pBEST-PT7extended-MGapt-UTR1-deGFP was a gift from Richard Murray (Addgene plasmid # 227646 ; http://n2t.net/addgene:227646 ; RRID:Addgene_227646) -
For your References section:
Metabolic perturbations to an E. coli-based cell-free system reveal a trade-off between transcription and translation. Kapasiawala M, Murray RM. bioRxiv 2023.03.22.533877 10.1101/2023.03.22.533877