pET29b-irp9 WT
(Plasmid
#87105)
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Purposeexpresses Irp9 WT, the salicylate synthase from Yersinia enterocolitica
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 87105 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET29b
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Backbone manufacturernovagen
- Backbone size w/o insert (bp) 5370
- Total vector size (bp) 6672
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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)DH5alpha
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Growth instructionsGrown at 37 degrees until OD600 ~ 1.0. Temperature turned to 18 degrees for 20 hours without induction
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameirp9 WT
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SpeciesYersinia enterocolitica
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Insert Size (bp)1302
- Promoter T7
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Tag
/ Fusion Protein
- his-tag (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NdeI (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer pET upstream
- 3′ sequencing primer T7 reverse (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
JACS 138 (2016) 9277-9293 PMC5029964
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:
pET29b-irp9 WT was a gift from Audrey Lamb (Addgene plasmid # 87105 ; http://n2t.net/addgene:87105 ; RRID:Addgene_87105) -
For your References section:
Redesign of MST enzymes to target lyase activity instead promotes mutase and dehydratase activities. Meneely KM, Luo Q, Lamb AL. Arch Biochem Biophys. 2013 Nov 1;539(1):70-80. doi: 10.1016/j.abb.2013.09.007. Epub 2013 Sep 19. 10.1016/j.abb.2013.09.007 PubMed 24055536