pRA1SEGFPTcIfm
(Plasmid
#193777)
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PurposeCassette 1: Expresses EGFP under the control of PR promoter, Cassette 2: Expresses frame-shifted CI under the control of PLTetO-1 promoter, pUC origin of replication, Ampicillin selection
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 193777 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepZ
- Backbone size w/o insert (bp) 2367
- Total vector size (bp) 4479
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Vector typeBacterial Expression, Synthetic 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)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameEGFP and frame-shifted CI in opposite orientation, controlled by separate promoters and terminators
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SpeciesBacteria
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Insert Size (bp)2112
- Promoter PR promoter and PLTetO-1
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site AvrII (unknown if destroyed)
- 3′ cloning site AvrII (unknown if destroyed)
- 5′ sequencing primer GTTTTGGAGCACG GAAAGAC (Common Sequencing Primers)
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:
pRA1SEGFPTcIfm was a gift from Sangram Bagh (Addgene plasmid # 193777 ; http://n2t.net/addgene:193777 ; RRID:Addgene_193777) -
For your References section:
A frame-shifted gene, which rescued its function by non-natural start codons and its application in constructing synthetic gene circuits. Sarkar K, Mukhopadhyay S, Bonnerjee D, Srivastava R, Bagh S. J Biol Eng. 2019 Mar 1;13:20. doi: 10.1186/s13036-019-0151-x. eCollection 2019. 10.1186/s13036-019-0151-x PubMed 30867677