pTRE/SP M87 N184X
(Plasmid
#92373)
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PurposeInducible expression of M87 N184X spastin in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 92373 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepTRE-Tight
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 2600
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Vector typeMammalian Expression
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 namespastin
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Alt nameSPAST
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Alt nameNM 014946
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SpeciesH. sapiens (human)
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Insert Size (bp)1668
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Mutation1-460 bp deleted, N184X
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Entrez GeneSPAST (a.k.a. ADPSP, FSP2, SPG4)
- Promoter Tet-responsive P tight
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SmaI (destroyed during cloning)
- 3′ cloning site BamHI (destroyed during cloning)
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
The endogenous M1 Kozak sequence was replaced with an optimal Kozak sequence to prevent leaky translation of M87 spastin. To detect spastin use an anti-spastin antibody.
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:
pTRE/SP M87 N184X was a gift from Peter Baas (Addgene plasmid # 92373 ; http://n2t.net/addgene:92373 ; RRID:Addgene_92373) -
For your References section:
Studies on truncating mutations of SPAST associated with Hereditary Spastic Paraplegia indicate greater accumulation and toxicity of the M1 isoform of spastin. Solowska JM, Rao AN, Baas PW. Mol Biol Cell. 2017 May 11. pii: mbc.E17-01-0047. doi: 10.1091/mbc.E17-01-0047. 10.1091/mbc.E17-01-0047 PubMed 28495799