Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
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 and Mitochondrially Encoded NADH Dehydrogenase 6 Kits (1) and many more products for this protein.
Showing 10 out of 22 products:
Human Polyclonal MT-ND6 Primary Antibody for IF (p), IHC (p) - ABIN751678
Wu, Zhang, Nickerson, Gao, Sun, Chen, Zhang, Zhang, Gao, Chen, Luo, Wang, Sun: Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma. in Neurobiology of disease 2015
Human Polyclonal MT-ND6 Primary Antibody for WB - ABIN2784118
Karamanlidis, Nascimben, Couper, Shekar, del Monte, Tian: Defective DNA replication impairs mitochondrial biogenesis in human failing hearts. in Circulation research 2010
This review focuses on the role of mitochondrial genes in causing LHON and therapeutics available for treating the disease. A systematic search has been adopted in various databases using the keywords "LHON," "mitochondria," "ND1 (show MT-ND1 Antibodies)," "ND4 (show MT-ND4 Antibodies)," "ND6," and "therapy" and the following review on mitochondrial genetics
Protein modeling revealed loss of function mutations of ND6 and COX (show COX8A Antibodies)-II proteins in malignant vs benign tumors
Liver MT-ND6 transcriptional activity and protein expression were decreased in nonalcoholic steatohepatitis, suggesting that the expression of this mitochondrial gene may play an important role in the disease progression.
Point mutations m.10191T>C in mitochondrial ND3 (show MT-ND3 Antibodies) gene, m.13513G>A in ND5 (show MT-ND5 Antibodies) gene and m.14,453G>A in ND6 gene were detected in three Chinese children with Leigh synrome dur to complex I deficiency.
These data suggested that the ND6 T14502C variant may modulate the phenotypic manifestation of the G11778A mutation in these Chinese pedigrees.
mitochondrial ND6 may have a role in Leber's hereditary optic neuropathy
Free radicals-mediated damage was studied in transmitochondrial cells harboring T14487C mutation in the ND6 gene of mtDNA.
Therefore, the coexistence of the A1555G mutation and T14484C mutations in this Chinese family indicate that the A1555G mutation may play a synergistic role in the phenotypic manifestation of LHON associated ND6 T14484C mutation.
T14484C and T14502C in ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.
G10680A mutation of ND4 (show MT-ND4 Antibodies) may play a synergistic role with the primary mutation T14484C of ND6, leading to the complete penetrance of Leber's hereditary optic neuropathy in the presenting family.
Data suggest that expression of ND6 in adipose tissue can be regulated by dietary factors; here, expression of ND6 in mitochondria of white adipose tissue is down-regulated in obesity caused by high-fat diet.
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 6