pET11a+D77R/T214V
(Plasmid
#66135)
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PurposeExpresses the D77R/T214V mutant of CYP119
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 66135 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET-11a
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Backbone manufacturerNovagen
- Backbone size w/o insert (bp) 5639
- Total vector size (bp) 6748
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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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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameCYP119
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Insert Size (bp)1109
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MutationD77R, T214V
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Entrez Genecyp119 (a.k.a. Saci_2081)
- Promoter T7 promoter
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)
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
We cloned the CYP119 gene from the cell suspension of S. solfataricus P1 strain (ATCC 35091).
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:
pET11a+D77R/T214V was a gift from Teruyuki Nagamune (Addgene plasmid # 66135 ; http://n2t.net/addgene:66135 ; RRID:Addgene_66135) -
For your References section:
Electron donation to an archaeal cytochrome P450 is enhanced by PCNA-mediated selective complex formation with foreign redox proteins. Suzuki R, Hirakawa H, Nagamune T. Biotechnol J. 2014 Dec;9(12):1573-81. doi: 10.1002/biot.201400007. Epub 2014 Jul 21. 10.1002/biot.201400007 PubMed 24924478