pIRESN2 H2B-GFP-uvr8at(2x)
(Plasmid
#44970)
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 44970 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepIRESneo2
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 5308
- Total vector size (bp) 9133
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
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 numberHigh Copy
Gene/Insert
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Gene/Insert nameH2B-GFP-UVR8(2x)
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Alt namehistone H2B
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Alt nameUV-B resistance 8
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SpeciesH. sapiens (human), A. thaliana (mustard weed)
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Insert Size (bp)3825
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Mutationtandem repeat of UVR8 (both have Methionine 1 deleted) linked by a flexible linker: GDSGDGKGGKGSGDGSGGDGSG
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GenBank IDNM_021058 NM_125781.3
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Entrez GeneUVR8 (a.k.a. AT5G63860, MGI19.7, MGI19_7, UVB-RESISTANCE 8)
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Entrez GeneH2BC21 (a.k.a. GL105, H2B, H2B-GL105, H2B.1, H2BE, H2BFQ, H2BGL105, H2BQ, HIST2H2BE)
- Promoter pCMV IE
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Tag
/ Fusion Protein
- internal GFP
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site AflII (destroyed during cloning)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer IRES-R (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.
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:
pIRESN2 H2B-GFP-uvr8at(2x) was a gift from Thanos Halazonetis (Addgene plasmid # 44970 ; http://n2t.net/addgene:44970 ; RRID:Addgene_44970) -
For your References section:
Ultraviolet-B-mediated induction of protein-protein interactions in mammalian cells. Crefcoeur RP, Yin R, Ulm R, Halazonetis TD. Nat Commun. 2013;4:1779. doi: 10.1038/ncomms2800. 10.1038/ncomms2800 PubMed 23653191