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PurposeExpression of human Parkin fused to eYFP
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Depositing Labs
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 61728 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneLZRS
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Vector typeMammalian Expression
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Selectable markersZeocin
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)Stbl2
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Growth instructionsSlow growing. May need additional incubation time.
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameParkin
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Alt namePark 2
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SpeciesH. sapiens (human)
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GenBank IDNM_004562
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Entrez GenePRKN (a.k.a. AR-JP, LPRS2, PARK2, PDJ)
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Tag
/ Fusion Protein
- eYFP (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (unknown if destroyed)
- 3′ cloning site EcoRI (unknown if destroyed)
- 5′ sequencing primer EGFP-C
- 3′ sequencing primer pCDH-Rev (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
Dr. Richard Youle provided YFP-Parkin (Addgene Plasmid 23955). Please note that the EBNA sequence may have ambiguous bases due to GC-rich regions.
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:
YFP-Parkin-IRES-zeo was a gift from Douglas Green & Stephen Tait (Addgene plasmid # 61728 ; http://n2t.net/addgene:61728 ; RRID:Addgene_61728) -
For your References section:
Widespread mitochondrial depletion via mitophagy does not compromise necroptosis. Tait SW, Oberst A, Quarato G, Milasta S, Haller M, Wang R, Karvela M, Ichim G, Yatim N, Albert ML, Kidd G, Wakefield R, Frase S, Krautwald S, Linkermann A, Green DR. Cell Rep. 2013 Nov 27;5(4):878-85. doi: 10.1016/j.celrep.2013.10.034. Epub 2013 Nov 21. 10.1016/j.celrep.2013.10.034 PubMed 24268776