This is a Validated Antibody Database (VAD) review about human ND1, based on 3 published articles (read how Labome selects the articles), using ND1 antibody in all methods. It is aimed to help Labome visitors find the most suited ND1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
ND1 synonym: MTND1; NADH dehydrogenase, subunit 1 (complex I); NADH dehydrogenase subunit 1

Abcam
rabbit monoclonal (EPR13466(2))
  • western blot; human; 1:1000; loading ...; fig 2
In order to examine nuclear mRNAs encoding subunits of mitochondrial complexes and mRNAs encoding energy metabolism-related enzymes in frontal cortex area 8 and the angular gyrus of middle-aged individuals, those with incidental Parkinson's disease, long-last, Abcam ND1 antibody (Abcam, ab181848) was used in western blot on human samples at 1:1000 (fig 2). Brain Pathol (2018) ncbi
Abnova
mouse polyclonal
  • western blot; human; fig 6
In order to analyze GTPBP3 defective expression in AMPK-mediated responses, Abnova ND1 antibody (Abnova, H00004535-A01) was used in western blot on human samples (fig 6). PLoS ONE (2015) ncbi
mouse polyclonal
  • western blot; human; 1:1000
Abnova ND1 antibody (Abnova, H00004535-A01) was used in western blot on human samples at 1:1000. JIMD Rep (2016) ncbi
Articles Reviewed
  1. Garcia Esparcia P, Koneti A, Rodríguez Oroz M, Gago B, del Río J, Ferrer I. Mitochondrial activity in the frontal cortex area 8 and angular gyrus in Parkinson's disease and Parkinson's disease with dementia. Brain Pathol. 2018;28:43-57 pubmed publisher
  2. Martínez Zamora A, Meseguer S, Esteve J, Villarroya M, Aguado C, Enríquez J, et al. Defective Expression of the Mitochondrial-tRNA Modifying Enzyme GTPBP3 Triggers AMPK-Mediated Adaptive Responses Involving Complex I Assembly Factors, Uncoupling Protein 2, and the Mitochondrial Pyruvate Carrier. PLoS ONE. 2015;10:e0144273 pubmed publisher
  3. Rafiq J, Duno M, Østergaard E, Ravn K, Vissing C, Wibrand F, et al. Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation. JIMD Rep. 2016;25:65-70 pubmed