pTRE2-Hyg-omMx1
(Plasmid
#52420)
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PurposeInducible expression (Tet-Off system) of the rainbow trout antiviral Mx1 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 | 52420 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepTRE2-Hyg
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 5298
- Total vector size (bp) 7164
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Vector typeMammalian Expression
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Selectable markersHygromycin
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)Top10
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameOncorhynchus mykiss interferon-induced GTP-binding protein Mx1 (mx1)
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SpeciesOncorhynchus mykiss
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Insert Size (bp)1866
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GenBank IDNM_001171901
- Promoter TRE2
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site MluI (not destroyed)
- 3′ cloning site SalI (not destroyed)
- 5′ sequencing primer TRE2F
- 3′ sequencing primer TRE2R (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
Addgene's quality control sequencing has found two amino acid residue substitutions, G431E and M577I, compared to the depositor's full sequence. These differences are believed to be natural inter-population polymorphisms and are not thought to affect plasmid function.
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:
pTRE2-Hyg-omMx1 was a gift from Bertrand Collet (Addgene plasmid # 52420 ; http://n2t.net/addgene:52420 ; RRID:Addgene_52420) -
For your References section:
Development of an in vitro system to measure the sensitivity to the antiviral Mx protein of fish viruses. Lester K, Hall M, Urquhart K, Gahlawat S, Collet B. J Virol Methods. 2012 Jun;182(1-2):1-8. doi: 10.1016/j.jviromet.2012.01.014. Epub 2012 Mar 1. 10.1016/j.jviromet.2012.01.014 PubMed 22405879