Mitochondrially Encoded NADH Dehydrogenase 5 (MT-ND5) 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 5 抗体 (59)Mitochondrially Encoded NADH Dehydrogenase 5 蛋白 (4)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
MT-ND5 4540 P03915
MT-ND5 26202  
MT-ND5    

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适于 Mitochondrially Encoded NADH Dehydrogenase 5 相互作用对的更多 ELISA 试剂盒

Human Mitochondrially Encoded NADH Dehydrogenase 5 (MT-ND5) interaction partners

  1. The m.13565C>T mutation in MTND5 causes defects in both mitochondrial oxidative metabolism and mitochondrial calcium sequestration in a MELAS syndrome fibroblasts.

  2. Mitochondrially encoded NADH dehydrogenase subunit, complex I extracts energy from NADH, produced by the oxidation of sugars and fats, and traps the energy in a potential difference or voltage across the mitochondrial inner membrane.

  3. Study demonstrates a link between p53 (显示 TP53 ELISA试剂盒) and Bcl-2 (显示 BCL2 ELISA试剂盒) proteins as regulators of ROS (显示 ROS1 ELISA试剂盒) production and cellular invasiveness, and reveals complex-I, especially ND5, as their functional target in lung tumor cells.

  4. Three mutations were significantly related to the presence of epilepsy. These mutations were found at the 8502, 11994, and 13,231 bp of mtDNA, which resulted in amino acid changes at the MT-ATP-8 (显示 MT-ATP8 ELISA试剂盒), MT-ND4 (显示 MT-ND4 ELISA试剂盒) and MT-ND5 genes.

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

  6. Mitochondrial ND5 12338T>C variant is associated with maternally inherited hypertrophic cardiomyopathy in a Chinese pedigree

  7. Mitochondrial DNA mutations in respiratory complex-I in never-smoker lung cancer patients contribute to lung cancer progression in association with EGFR (显示 EGFR ELISA试剂盒) gene mutation.

  8. ND4 (显示 MT-ND4 ELISA试剂盒) G11696A and ND5 T12338C mutation is likely associated with Leber's hereditary optic neuropathy in two Chinese families

  9. Patients with ND5*13513 G to A mutation may have a characteristic clinical course and ND5 *13513 G to A might be a preferential candidate mutation of Leigh syndrome.

  10. these results suggest that the MT-ND1 (显示 MT-ND1 ELISA试剂盒) and MT-ND5 genes are mutational hotspots for Chinese families with suspected LHON lacking the common primary mutations.

Mitochondrially Encoded NADH Dehydrogenase 5 (MT-ND5) 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-ND5

  • mitochondrial NADH-ubiquinone oxidoreductase chain 5 (mt:ND5) 抗体
  • mitochondrially encoded NADH dehydrogenase 5 (MT-ND5) 抗体
  • NADH dehydrogenase 5, mitochondrial (mt-Nd5) 抗体
  • NADH dehydrogenase subunit 5 (ND5) 抗体
  • NADH dehydrogenase subunit 5 (nad5) 抗体
  • NADH dehydrogenase, subunit 5 (nad5) 抗体
  • MTND5 抗体
  • NADH5 抗体

Protein level used designations for MT-ND5

NADH dehydrogenase subunit 5

GENE ID SPECIES
192478 Drosophila melanogaster
4540 Homo sapiens
26202 Rattus norvegicus
804484 Canis lupus familiaris
807642 Gallus gallus
808511 Sus scrofa
808224 Oryctolagus cuniculus
2565703 Caenorhabditis elegans
3371313 Arabidopsis thaliana
808209 Branchiostoma lanceolatum
1734025 Acanthamoeba castellanii
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