MSCVneo-HA-ER-Hoxb8
(Plasmid
#222291)
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PurposeThe most commonly used plasmid for the generation of ER-Hoxb8 conditionally immortalized myeloid cell lines.
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Depositing Labs
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 222291 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneMSCVneo
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Backbone manufacturerTakeda
- Backbone size w/o insert (bp) 6436
- Total vector size (bp) 8155
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Vector typeMammalian Expression, Retroviral
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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)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameER-Hoxb8
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Alt nameHuman estrogen receptor alpha hormone binding domain fused to murine hoxb8
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Alt nameThe hormone binding domain = amino acids 282-595
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SpeciesH. sapiens (human), M. musculus (mouse)
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Insert Size (bp)1677
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MutationThe estrogen receptor hormone binding domain contains the G400V point mutation
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GenBank ID2099, 15416
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Entrez GeneESR1 (a.k.a. ER, ESR, ESRA, ESTRR, Era, NR3A1)
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Entrez GeneHoxb8 (a.k.a. Hox-2.4)
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Tag
/ Fusion Protein
- HA (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoR1 (unknown if destroyed)
- 3′ cloning site Xho1 (unknown if destroyed)
- 5′ sequencing primer None (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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:
MSCVneo-HA-ER-Hoxb8 was a gift from Mark Kamps & David Sykes (Addgene plasmid # 222291 ; http://n2t.net/addgene:222291 ; RRID:Addgene_222291) -
For your References section:
Quantitative production of macrophages or neutrophils ex vivo using conditional Hoxb8. Wang GG, Calvo KR, Pasillas MP, Sykes DB, Hacker H, Kamps MP. Nat Methods. 2006 Apr;3(4):287-93. 10.1038/nmeth865 PubMed 16554834