pET15T+1X
(Plasmid
#108188)
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PurposePCNA1-PdX fusion protein
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 108188 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET-15b
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Backbone manufacturerMerck Millipore
- Backbone size w/o insert (bp) 5724
- Total vector size (bp) 6888
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Modifications to backboneA SapI site was mutated. A TEV protease recognition site was inserted between a thrombin recognition site and an NdeI site.
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Vector typeBacterial 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)DH5alpha
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Growth instructionsSupplement with 1% glucose is recommended to suppress leaky expression.
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Copy numberLow Copy
Gene/Insert
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Gene/Insert namePCNA1-PdX fusion protein
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SpeciesSynthetic; Sulfolobus solfataricus P2, Pseudomonas putida
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Insert Size (bp)1164
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MutationC73S/C85S (PdX)
- Promoter T7 promoter
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Tag
/ Fusion Protein
- His6 tag (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NdeI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer T7 Terminal (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byMasahiro Goto, Kyushu University
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:
pET15T+1X was a gift from Teruyuki Nagamune (Addgene plasmid # 108188 ; http://n2t.net/addgene:108188 ; RRID:Addgene_108188) -
For your References section:
Artificial Self-Sufficient Cytochrome P450 Containing Multiple Auxiliary Proteins Demonstrates Improved Monooxygenase Activity. Haga T, Hirakawa H, Nagamune T. Biotechnol J. 2018 Dec;13(12):e1800088. doi: 10.1002/biot.201800088. Epub 2018 Aug 14. 10.1002/biot.201800088 PubMed 30039932