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PurposeEncodes a NADPH dependent blue fluorescent protein expressed under a strong promoter and strong RBS without His-tagged.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 63847 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepQE-30
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Vector typeBacterial Expression
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH10B
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namemBFP
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SpeciesSynthetic
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Insert Size (bp)747
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MutationPromoter and RBS was swapped. His-tag was removed from pQE-mBFP(Cat-). Ampicillin marker was swapped to Kanamycin.
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site unknown (unknown if destroyed)
- 3′ cloning site unknown (unknown if destroyed)
- 5′ sequencing primer pBRforEco (Common Sequencing Primers)
Resource Information
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Article Citing this Plasmid
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:
pCN-mBFP was a gift from Howard Salis (Addgene plasmid # 63847 ; http://n2t.net/addgene:63847 ; RRID:Addgene_63847) -
For your References section:
Rational design of a synthetic Entner-Doudoroff pathway for improved and controllable NADPH regeneration. Ng CY, Farasat I, Maranas CD, Salis HM. Metab Eng. 2015 May;29:86-96. doi: 10.1016/j.ymben.2015.03.001. Epub 2015 Mar 10. 10.1016/j.ymben.2015.03.001 PubMed 25769287