Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6) ELISA试剂盒

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 6 抗体 (22)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
MT-ND6 4541 P03923
小鼠 MT-ND6 MT-ND6 17722 P03925
大鼠 MT-ND6 MT-ND6 26203  
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5.86 pg/mL 23.44-1500 pg/mL Typical standard curve 96 Tests Log in to see 15至18个工作日
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适于 Mitochondrially Encoded NADH Dehydrogenase 6 相互作用对的更多 ELISA 试剂盒

Human Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6) interaction partners

  1. Protein modeling revealed loss of function mutations of ND6 and COX (显示 COX8A ELISA试剂盒)-II proteins in malignant vs benign tumors

  2. 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.

  3. Point mutations m.10191T>C in mitochondrial ND3 (显示 MT-ND3 ELISA试剂盒) gene, m.13513G>A in ND5 (显示 MT-ND5 ELISA试剂盒) gene and m.14,453G>A in ND6 gene were detected in three Chinese children with Leigh synrome dur to complex I deficiency.

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

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

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

  7. 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.

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

  9. G10680A mutation of ND4 (显示 MT-ND4 ELISA试剂盒) 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.

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

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

  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) 抗原简介

Antigen Summary

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).

Gene names and symbols associated with MT-ND6

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

Protein level used designations for MT-ND6

NADH dehydrogenase subunit 6

GENE ID SPECIES
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
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