pCI-MS2V5-PABPC1 MLLEmut M161A/D165K
(Plasmid
#65810)
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Purposeexpression of PABPC1-MS2 fusion, double mutant.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 65810 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCI-neo
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Backbone manufacturerPromega
- Backbone size w/o insert (bp) 4572
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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 numberUnknown
Gene/Insert
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Gene/Insert namePABPC1
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Alt namepoly(A) binding protein, cytoplasmic 4
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SpeciesH. sapiens (human)
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MutationMLLEmut M161A/D165K
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Entrez GenePABPC4 (a.k.a. APP-1, APP1, PABP4, iPABP)
- Promoter CMV
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Tags
/ Fusion Proteins
- MS2 stem loops (N terminal on insert)
- V5 (N terminal on insert)
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer CMV-F
- 3′ sequencing primer EBV-R (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:
pCI-MS2V5-PABPC1 MLLEmut M161A/D165K was a gift from Niels Gehring (Addgene plasmid # 65810 ; http://n2t.net/addgene:65810 ; RRID:Addgene_65810) -
For your References section:
The interaction of cytoplasmic poly(A)-binding protein with eukaryotic initiation factor 4G suppresses nonsense-mediated mRNA decay. Fatscher T, Boehm V, Weiche B, Gehring NH. RNA. 2014 Oct;20(10):1579-92. doi: 10.1261/rna.044933.114. Epub 2014 Aug 21. 10.1261/rna.044933.114 PubMed 25147240