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PurposeLentiviral expression vector for TAZ S89A mutant with N-terminal FLAG and His tags
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 52084 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepLenti-EF-ires-blast
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Modifications to backbonepLenti-EF-FH-TAZ S89A was constructed by subcloning NheI/SalI fragment from pCIneoFH-TAZ S89A into pLenti-EF-ires-blast vector. TAZ insert was amplified by PCR, cut with EcoRI and XhoI and ligated into EcoRI and Sall sites of pLenti-EF-ires-blast vector.
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Vector typeMammalian Expression, Lentiviral
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Selectable markersBlasticidin
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature30°C
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Growth Strain(s)NEB Stable
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameTAZ S89A
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Alt nameTranscriptional co-activator with PDZ-binding motif
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Alt nameWWTR1
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SpeciesH. sapiens (human)
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MutationS89A
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Entrez GeneWWTR1 (a.k.a. TAZ)
- Promoter EF1a
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Tags
/ Fusion Proteins
- FLAG (N terminal on backbone)
- His (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site SalI (destroyed during cloning)
- 5′ sequencing primer EF1a-F
- 3′ sequencing primer pBABE-3 (Common Sequencing Primers)
Resource Information
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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.
Depositor Comments
Please note that TAZ has a Sall site present within the coding region.
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:
pLenti-EF-FH-TAZ S89A-ires-blast was a gift from Yutaka Hata (Addgene plasmid # 52084 ; http://n2t.net/addgene:52084 ; RRID:Addgene_52084) -
For your References section:
Screening with a novel cell-based assay for TAZ activators identifies a compound that enhances myogenesis in C2C12 cells and facilitates muscle repair in the muscle injury model. Yang Z, Nakagawa K, Sarkar A, Maruyama J, Iwasa H, Bao Y, Ishigami-Yuasa M, Ito S, Kagechika H, Hata S, Nishina H, Abe S, Kitagawa M, Hata Y. Mol Cell Biol. 2014 Feb 18. 10.1128/MCB.01346-13 PubMed 24550007