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PurposeFLAG-tagged overexpression
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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 | 87931 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepRK5
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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 nameATP6Vod1
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Alt nameP39; VATX; VMA6; ATP6D; ATP6DV; VPATPD
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SpeciesH. sapiens (human)
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Insert Size (bp)1056
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GenBank IDNM_004691.4
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Entrez GeneATP6V0D1 (a.k.a. ATP6D, ATP6DV, P39, VATX, VMA6, VPATPD)
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Tag
/ Fusion Protein
- FLAG (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Sal1 (not destroyed)
- 3′ cloning site Not1 (not destroyed)
- 5′ sequencing primer SP6 : ATT TAG GTG ACA CTA TAG
- 3′ sequencing primer pRK5-3': TGT AAC CAT TAT AAG CTG (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.
Depositor Comments
Human cDNA ATP6V0D1 purchased from Open Biosystems
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:
pRK5-FLAG-ATP6V0D1 was a gift from David Sabatini (Addgene plasmid # 87931 ; http://n2t.net/addgene:87931 ; RRID:Addgene_87931) -
For your References section:
mTORC1 senses lysosomal amino acids through an inside-out mechanism that requires the vacuolar H-ATPase. Zoncu R, Bar-Peled L, Efeyan A, Wang S, Sancak Y, Sabatini DM. Science. 2011 Nov 4;334(6056):678-83. 10.1126/science.1207056 PubMed 22053050