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PurposeFusion protein used to visualise mitochondria upon the addition of Halo specific dye, has hygromycin selection
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 111626 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMIH/MSCV-IRES-hygro
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Backbone manufacturerMark Van Delft
- Backbone size w/o insert (bp) 6969
- Total vector size (bp) 8340
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Vector typeMammalian Expression, Retroviral
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Selectable markersHygromycin
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 numberUnknown
Gene/Insert
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Gene/Insert nameTOMM20
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SpeciesM. musculus (mouse)
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Insert Size (bp)2782
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GenBank IDNM_014765.2
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Entrez GeneTomm20 (a.k.a. 1810060K07Rik, BB284719, Gm19268, MAS20, MOM19, TOM20, mKIAA0016)
- Promoter MSCV
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Tag
/ Fusion Protein
- HaloTag (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BglII (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer gaacctcctcgttcgaccc (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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Addgene Notes
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A portion of this plasmid was derived from a plasmid made byBackbone provided by Dr Mark Van Delft & Prof David Huang. TOMM20 insert synthesised by Genscript (NM_014765.2). HaloTag purchased from Promega #G7721 pHTN.
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Article 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.
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:
pMIH-TOMM20-Halo was a gift from Benjamin Kile (Addgene plasmid # 111626 ; http://n2t.net/addgene:111626 ; RRID:Addgene_111626) -
For your References section:
BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis. McArthur K, Whitehead LW, Heddleston JM, Li L, Padman BS, Oorschot V, Geoghegan ND, Chappaz S, Davidson S, San Chin H, Lane RM, Dramicanin M, Saunders TL, Sugiana C, Lessene R, Osellame LD, Chew TL, Dewson G, Lazarou M, Ramm G, Lessene G, Ryan MT, Rogers KL, van Delft MF, Kile BT. Science. 2018 Feb 23;359(6378). pii: 359/6378/eaao6047. doi: 10.1126/science.aao6047. 10.1126/science.aao6047 PubMed 29472455