This is a Validated Antibody Database (VAD) review about human COQ8A, based on 3 published articles (read how Labome selects the articles), using COQ8A antibody in all methods. It is aimed to help Labome visitors find the most suited COQ8A antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
COQ8A synonym: ADCK3; ARCA2; CABC1; COQ10D4; COQ8; SCAR9; atypical kinase COQ8A, mitochondrial; aarF domain-containing protein kinase 3; atypical kinase ADCK3, mitochondrial; chaperone activity of bc1 complex-like, mitochondrial; chaperone, ABC1 activity of bc1 complex homolog; coenzyme Q protein 8A; coenzyme Q8 homolog

Abnova
mouse monoclonal (7G1)
  • western blot; human; 1:100; loading ...; fig 5b
In order to examine coenzyme Q10 levels in patients with multiple system atrophy, Abnova COQ8A antibody (Abnova, H00056997-M04A) was used in western blot on human samples at 1:100 (fig 5b). J Neuropathol Exp Neurol (2016) ncbi
mouse monoclonal (7G1)
  • western blot; human; 1:100; fig s5
In order to compare two mouse models with a genetic modification in the Coq9 gene, Abnova COQ8A antibody (Abnova, H00056997-M04A) was used in western blot on human samples at 1:100 (fig s5). EMBO Mol Med (2015) ncbi
Invitrogen
rabbit polyclonal
  • western blot; human; 1:1000; loading ...; fig 6c
In order to study the effects of coenzyme Q deficiency in human skin fibroblasts, Invitrogen COQ8A antibody (Thermo Scientific, PA5-13906) was used in western blot on human samples at 1:1000 (fig 6c). EMBO Mol Med (2017) ncbi
Articles Reviewed
  1. Ziosi M, Di Meo I, Kleiner G, Gao X, Barca E, Sanchez Quintero M, et al. Coenzyme Q deficiency causes impairment of the sulfide oxidation pathway. EMBO Mol Med. 2017;9:96-111 pubmed publisher
  2. Barca E, Kleiner G, Tang G, Ziosi M, Tadesse S, Masliah E, et al. Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum. J Neuropathol Exp Neurol. 2016;75:663-72 pubmed publisher
  3. Luna Sánchez M, Díaz Casado E, Barca E, Tejada M, Montilla García Ã, Cobos E, et al. The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene. EMBO Mol Med. 2015;7:670-87 pubmed publisher