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Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Additionally we are shipping Mitochondrially Encoded NADH Dehydrogenase 1 Kits (17) and Mitochondrially Encoded NADH Dehydrogenase 1 Proteins (7) and many more products for this protein.
Showing 10 out of 33 products:
Human Polyclonal MT-ND1 Primary Antibody for ELISA, WB - ABIN561868
Karamanlidis, Nascimben, Couper, Shekar, del Monte, Tian: Defective DNA replication impairs mitochondrial biogenesis in human failing hearts. in Circulation research 2010
Show all 3 references for ABIN561868
Human Polyclonal MT-ND1 Primary Antibody for IHC, ELISA - ABIN1535071
Anderson, Bankier, Barrell, de Bruijn, Coulson, Drouin, Eperon, Nierlich, Roe, Sanger, Schreier, Smith, Staden, Young: Sequence and organization of the human mitochondrial genome. in Nature 1981
The present study revealed no association between MS and T4216C variation in the ND1 mtDNA gene in the Iranian population.
ND1 T3866C mutation is associated with Chinese families with Leber's hereditary optic neuropathy.
To investigate the pathophysiology of Leber's hereditary optic neuropathy (LHON), a cohort of 1164 Han Chinese subjects with LHON were screened for ND1 G3460A mutation.
m.3460G>A/MT-ND1 mutation caused only a reduction in mitochondrial complex I(CI) activity, whereas the m.3571insC/MT-ND1 and the m.3243A>G/MT-TL1 (show TNFSF15 Antibodies) mutations induced a severe structural and functional CI alteration.
Novel mutations m.3959G>A and m.3995A>G in mitochondrial gene MT-ND1 associated with MELAS.
In Sherpa people, 2 mutations are ND1 mutants. One of them was reported as the primary mutation for Leber's hereditary optic neuropathy suggesting a certain effect on Complex I function and might be important in the altitude adaptation for Sherpa people.
we describe here a heteroplasmic mutation in the MT-ND1 gene that strongly suggest to cause epileptic encephalopathy: West syndrome (WS) patient with unidentified etiology that evolved to Lennox-Gastaut syndrome.
A statistically significant association of the T4216C mutation in ND1 (p < 0.05) between patients suffering recurrent pregnancy loss and controls, which are 30% and 11%, respectively.
BRN2 is a higher level regulator than ASCL1 and ND1 and BRN2 might be involved in aggressiveness of small cell lung cancer.
These data suggest that the four early Complex I assembly factors have non-redundant functions in the assembly of a module that docks and stabilizes newly synthesized ND1.
Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone (By similarity).
NADH dehydrogenase subunit 1
, NADH-ubiquinone oxidoreductase chain 1
, PPIase A
, cyclophilin A
, cyclosporin A-binding protein
, peptidyl-prolyl cis-trans isomerase A
, rotamase A