Use your antibodies-online credentials, if available.
Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. 再加上，我们可以发Mitochondrially Encoded NADH Dehydrogenase 1 试剂盒 (16) 和 Mitochondrially Encoded NADH Dehydrogenase 1 蛋白 (7)和数多这个蛋白质的别的产品。
Showing 10 out of 36 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 Pubmed References
The MT-ND1 m.3635G>A mutation has resulted in decreased efficiency of ATP synthesis.
the MT-ND1 gene is a hot spot for mutations associated with LHON.
ND1 genetic polymorphisms associated with breast cancer in Mizoram mongloid population.
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 (显示 TNFSF15 抗体) 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.
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