Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6) ELISA Kits

Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Zusätzlich bieten wir Ihnen Mitochondrially Encoded NADH Dehydrogenase 6 Antikörper (35) und und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
MT-ND6 4541 P03923
Anti-Maus MT-ND6 MT-ND6 17722 P03925
Anti-Ratte MT-ND6 MT-ND6 26203  
Direkt bei antikoerper-online bestellen
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Online bestellen
  • orders@antikoerper-online.de

Top Mitochondrially Encoded NADH Dehydrogenase 6 ELISA Kits auf antikoerper-online.de

Showing 1 out of 1 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Lieferzeit Preis Details
Human 5.86 pg/mL 23.44-1500 pg/mL Typical standard curve 96 Tests 15 bis 18 Tage
$910.56
Details

Weitere ELISA Kits für Mitochondrially Encoded NADH Dehydrogenase 6 Interaktionspartner

Human Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6) Interaktionspartner

  1. Our study suggests to include haplogroup T as a possible genetic background influencing LHON penetrance and to consider the increase of mtDNA copy number as a protective factor from vision loss regardless the hetero/homoplasmic status of LHON primary mutations.

  2. Study identify a significant down-expression of MT-ND6 in men with Klinefelter syndrome.

  3. The molecular diagnostics by the whole exome sequencing showed a novel de novo (c.1374-2A>C) mutation in the KRT10 gene responsible for the development of IWC (KRT10 defect was confirmed by immunofluorescent study). Concurrently, the m.14484T>C mutation in mitochondrial MTND6 gene (characteristic for Leber's hereditary optic neuropathy or LHON) was detected in patient, his mother and brother

  4. 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," "ND4," "ND6," and "therapy" and the following review on mitochondrial genetics

  5. In this study, 27.5% mutation was detected in North Indian LHON families. These results suggest that m.G11778A mutation is more frequent in this population. The results of the present study are compatible with studies of an Asian population and Northern European population.

  6. Protein modeling revealed loss of function mutations of ND6 and COX-II proteins in malignant vs benign tumors

  7. 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.

  8. This study shows that m.14484T>C arose independently in a different mtDNA haplogroup and ethnic background in India, which may influence the clinical expression of the disease.

  9. Point mutations m.10191T>C in mitochondrial ND3 gene, m.13513G>A in ND5 gene and m.14,453G>A in ND6 gene were detected in three Chinese children with Leigh synrome dur to complex I deficiency.

  10. These results suggest that a different set of LHON-causing mutations is present in the South Indian population than in the European population

  11. These data suggested that the ND6 T14502C variant may modulate the phenotypic manifestation of the G11778A mutation in these Chinese pedigrees.

  12. the G14459A mutation is a candidate mutation for maternally inherited dystonia

  13. novel mitochondrial DNA nucleotide transversion, C14482A (M64I) was found to cause Leber's hereditary optic neuropathy with visual recovery

  14. mitochondrial ND6 may have a role in Leber's hereditary optic neuropathy

  15. Free radicals-mediated damage was studied in transmitochondrial cells harboring T14487C mutation in the ND6 gene of mtDNA.

  16. 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.

  17. T14484C and T14502C in ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.

  18. G10680A mutation of ND4 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.

  19. Molecular analysis has led to identification of the known T14502C mutation in ND6 gene in Chinese families with Leber's hereditary optic neuropathy.

  20. missense mutation 14487T>C resulted in severe encephalopathies ranging from infantile Leigh syndrome to adult-onset progressive myoclonic epilepsy with dystonia in a five-generation family

Mouse (Murine) Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6) Interaktionspartner

  1. 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.

Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6) Antigen-Profil

Beschreibung des Gens

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).

Genbezeichner und Symbole assoziert mit MT-ND6

  • mitochondrial NADH-ubiquinone oxidoreductase chain 6 (mt:ND6) Antikörper
  • NADH dehydrogenase, subunit 6 (complex I) (ND6) Antikörper
  • NADH dehydrogenase subunit 6 (ND6) Antikörper
  • NADH dehydrogenase subunit 6 (nad6) Antikörper
  • NADH dehydrogenasesubunit 6 (nad6) Antikörper
  • MTND6 Antikörper
  • NADH6 Antikörper

Bezeichner auf Proteinebene für MT-ND6

NADH dehydrogenase subunit 6

GENE ID SPEZIES
192479 Drosophila melanogaster
4541 Homo sapiens
17722 Mus musculus
26203 Rattus norvegicus
3283888 Bos taurus
804485 Canis lupus familiaris
807640 Gallus gallus
808512 Sus scrofa
808223 Oryctolagus cuniculus
2565699 Caenorhabditis elegans
808211 Branchiostoma lanceolatum
807664 Ascaris suum
814580 Arabidopsis thaliana
807967 Locusta migratoria
1734024 Acanthamoeba castellanii
Ausgewählte Anbieter für Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6) ELISA Kits
Haben Sie etwas anderes gesucht?