pET-TRSter
(Plasmid
#78865)
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PurposeExpresses rat Thioredoxin Reductase using an open reading frame in fusion with a mutated E. coli-type SECIS element
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 78865 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET-24(s)+
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Backbone manufacturerNovagen Inc.
- Total vector size (bp) 6796
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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 instructionsExpression host BL21(DE3)
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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameThioredoxin Reductase
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Alt nameTxnrd1 (a.k.a. TR1 or TrxR1)
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SpeciesR. norvegicus (rat)
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Insert Size (bp)3450
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GenBank IDNM_031614.2
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Entrez GeneTxnrd1 (a.k.a. Tr)
- Promoter T7lac
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Tag
/ Fusion Protein
- Mutated E. coli-type SECIS element (3’ end of insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NcoI (unknown if destroyed)
- 3′ cloning site SalI (unknown if destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer T7 terminal (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.
Depositor Comments
Additional article references: PubMed PMID: 15345395
A > G (nucleotide) at bp 4 compared to NM_031614.2, which results in N2D compared to NP_113802.2.
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:
pET-TRSter was a gift from Elias Arnér (Addgene plasmid # 78865 ; http://n2t.net/addgene:78865 ; RRID:Addgene_78865) -
For your References section:
High-level expression in Escherichia coli of selenocysteine-containing rat thioredoxin reductase utilizing gene fusions with engineered bacterial-type SECIS elements and co-expression with the selA, selB and selC genes. Arner ES, Sarioglu H, Lottspeich F, Holmgren A, Bock A. J Mol Biol. 1999 Oct 8;292(5):1003-16. 10.1006/jmbi.1999.3085 PubMed 10512699