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PurposeGenerating lentiviruses to express Dlx2 and hygromycin resistance
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 97330 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneTetO-FUW
- Backbone size w/o insert (bp) 8373
- Total vector size (bp) 11018
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Vector typeLentiviral
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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)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameDLX2
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SpeciesM. musculus (mouse)
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Insert Size (bp)2654
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GenBank IDNM_010054.2
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Entrez GeneDlx2 (a.k.a. DII A, Dlx-2, Tes-1)
- Promoter TetO
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoR1 (not destroyed)
- 3′ cloning site PacI (not destroyed)
- 5′ sequencing primer LNCX
- 3′ sequencing primer WPRE-R (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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Articles 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:
DLX2-hygro was a gift from Marius Wernig (Addgene plasmid # 97330 ; http://n2t.net/addgene:97330 ; RRID:Addgene_97330) -
For your References section:
Generation of pure GABAergic neurons by transcription factor programming. Yang N, Chanda S, Marro S, Ng YH, Janas JA, Haag D, Ang CE, Tang Y, Flores Q, Mall M, Wapinski O, Li M, Ahlenius H, Rubenstein JL, Chang HY, Buylla AA, Sudhof TC, Wernig M. Nat Methods. 2017 May 15. doi: 10.1038/nmeth.4291. 10.1038/nmeth.4291 PubMed 28504679