Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation)

Atlas Antibodies

Catalog No.:
ATL-HPA043475-100
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Protein Description: voltage-dependent anion channel 2
Gene Name: VDAC2
Alternative Gene Name:
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000021771: 65%, ENSRNOG00000013505: 62%
Entrez Gene ID: 7417
Uniprot ID: P45880
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.

Product Specifications
Application WB, ICC, IHC
Reactivity Human
Clonality Polyclonal
Host Rabbit
Immunogen MATHGQTCARPMCIPPSYADLGKAAR
Gene Sequence MATHGQTCARPMCIPPSYADLGKAAR
Gene ID - Mouse ENSMUSG00000021771
Gene ID - Rat ENSRNOG00000013505
Buffer 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.

Documents & Links for Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation)
Datasheet Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation) Datasheet (External Link)
Vendor Page Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation) at Atlas Antibodies

Documents & Links for Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation)
Datasheet Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation) Datasheet (External Link)
Vendor Page Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation)
Citations for Anti VDAC2 pAb (ATL-HPA043475 w/enhanced validation) – 2 Found
Ydfors, Mia; Hughes, Meghan C; Laham, Robert; Schlattner, Uwe; Norrbom, Jessica; Perry, Christopher G R. Modelling in vivo creatine/phosphocreatine in vitro reveals divergent adaptations in human muscle mitochondrial respiratory control by ADP after acute and chronic exercise. The Journal Of Physiology. 2016;594(11):3127-40.  PubMed
Elouej, Sahar; Harhouri, Karim; Le Mao, Morgane; Baujat, Genevieve; Nampoothiri, Sheela; Kayserili, Hϋlya; Menabawy, Nihal Al; Selim, Laila; Paneque, Arianne Llamos; Kubisch, Christian; Lessel, Davor; Rubinsztajn, Robert; Charar, Chayki; Bartoli, Catherine; Airault, Coraline; Deleuze, Jean-François; Rötig, Agnes; Bauer, Peter; Pereira, Catarina; Loh, Abigail; Escande-Beillard, Nathalie; Muchir, Antoine; Martino, Lisa; Gruenbaum, Yosef; Lee, Song-Hua; Manivet, Philippe; Lenaers, Guy; Reversade, Bruno; Lévy, Nicolas; De Sandre-Giovannoli, Annachiara. Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology. Nature Communications. 2020;11(1):4589.  PubMed