MSCV-mouse Ezh2 delta SETdomain-IRES-GFP
(Plasmid
#91885)
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PurposeRetroviral expression of mouse Ezh2 with a SET domain deletion
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 91885 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneMSCV-IRES-GFP
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Backbone manufacturerTannishtha Reya (Addgene #20672)
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Vector typeMammalian Expression, Retroviral
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Selectable markersEGFP
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)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameEzh2
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SpeciesM. musculus (mouse)
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MutationSET domain deleted
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Entrez GeneEzh2 (a.k.a. Enx-1, Enx1h, KMT6, mKIAA4065)
- Promoter MMLV gag
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Tag
/ Fusion Protein
- IRES-EGFP (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BglI (unknown if destroyed)
- 3′ cloning site XhoI (unknown if destroyed)
- 5′ sequencing primer pLXSN 5' (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byMSCV-Flag-mut-Ezh2-ΔSET-Hydromycin was purchased from Addgene (Cat# 49403)
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:
MSCV-mouse Ezh2 delta SETdomain-IRES-GFP was a gift from Martine Roussel (Addgene plasmid # 91885 ; http://n2t.net/addgene:91885 ; RRID:Addgene_91885) -
For your References section:
Inactivation of Ezh2 Upregulates Gfi1 and Drives Aggressive Myc-Driven Group 3 Medulloblastoma. Vo BT, Li C, Morgan MA, Theurillat I, Finkelstein D, Wright S, Hyle J, Smith SM, Fan Y, Wang YD, Wu G, Orr BA, Northcott PA, Shilatifard A, Sherr CJ, Roussel MF. Cell Rep. 2017 Mar 21;18(12):2907-2917. doi: 10.1016/j.celrep.2017.02.073. 10.1016/j.celrep.2017.02.073 PubMed 28329683