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Purposeexpresses lambdaN-HA-tagged XRN1 in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 66596 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepLNHA-C1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4174
- Total vector size (bp) 9295
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Modifications to backboneExchanged the EGFP tag from pEGFP-C1 by a lambdaN-HA-tag
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Vector typeMammalian 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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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameXRN1
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Alt nameSEP1
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SpeciesH. sapiens (human)
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Insert Size (bp)5121
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GenBank IDNM_019001
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Entrez GeneXRN1 (a.k.a. SEP1)
- Promoter CMV
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Tag
/ Fusion Protein
- lambdaN-HA (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SacII (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer CMV for (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.
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:
pLNHA-C1-HsXRN1 was a gift from Elisa Izaurralde (Addgene plasmid # 66596 ; http://n2t.net/addgene:66596 ; RRID:Addgene_66596) -
For your References section:
A direct interaction between DCP1 and XRN1 couples mRNA decapping to 5' exonucleolytic degradation. Braun JE, Truffault V, Boland A, Huntzinger E, Chang CT, Haas G, Weichenrieder O, Coles M, Izaurralde E. Nat Struct Mol Biol. 2012 Dec;19(12):1324-31. doi: 10.1038/nsmb.2413. Epub 2012 Nov 11. 10.1038/nsmb.2413 PubMed 23142987