pcDNA3.1 Mfn2-HA S27A
(Plasmid
#139193)
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PurposeExpresses C-terminal HA tagged human Mfn2 S27A 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 | 139193 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA3.1
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Backbone manufacturerThermo Fisher Scientific
- Backbone size w/o insert (bp) 5428
- Total vector size (bp) 7766
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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 numberHigh Copy
Gene/Insert
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Gene/Insert nameMFN2
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Alt nameMitofusin 2
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SpeciesH. sapiens (human)
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Insert Size (bp)2273
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MutationSerine 27 to Alanine
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GenBank IDNM_014874
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Entrez GeneMFN2 (a.k.a. CMT2A, CMT2A2, CMT2A2A, CMT2A2B, CPRP1, HMSN6A, HSG, MARF, MSL)
- Promoter CMV promoter
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Tag
/ Fusion Protein
- 3HA (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer T7 promoter primer
- 3′ sequencing primer pCDNA3.1/BGH (Common Sequencing Primers)
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:
pcDNA3.1 Mfn2-HA S27A was a gift from Allan Weissman (Addgene plasmid # 139193 ; http://n2t.net/addgene:139193 ; RRID:Addgene_139193) -
For your References section:
Stress-induced phosphorylation and proteasomal degradation of mitofusin 2 facilitates mitochondrial fragmentation and apoptosis. Leboucher GP, Tsai YC, Yang M, Shaw KC, Zhou M, Veenstra TD, Glickman MH, Weissman AM. Mol Cell. 2012 Aug 24;47(4):547-57. doi: 10.1016/j.molcel.2012.05.041. Epub 2012 Jun 28. 10.1016/j.molcel.2012.05.041 PubMed 22748923