Mitochondrially Encoded NADH Dehydrogenase 1 (MT-ND1) 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 1 抗体 (36)Mitochondrially Encoded NADH Dehydrogenase 1 蛋白 (7)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
MT-ND1 4535 P03886
MT-ND1 26193  
MT-ND1 17716 P03888
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产品编号 适用 灵敏度 范围 图像 规格 供应商 交付 价格 详细
小鼠 0.115 ng/mL 0.31-20 ng/mL 96 Tests Log in to see 13至16个工作日
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大鼠 0.068 ng/mL 0.156-10 ng/mL 96 Tests Log in to see 15至17个工作日
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0.068 ng/mL 0.156-10 ng/mL Typical Standard Curve 96 Tests Log in to see 15至17个工作日
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小鼠 0.115 ng/mL 0.312 ng/mL - 20 ng/mL   96 Tests Log in to see 8至12个工作日
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大鼠 0.058 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Log in to see 8至12个工作日
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适于 Mitochondrially Encoded NADH Dehydrogenase 1 相互作用对的更多 ELISA 试剂盒

Human Mitochondrially Encoded NADH Dehydrogenase 1 (MT-ND1) interaction partners

  1. The MT-ND1 m.3635G>A mutation has resulted in decreased efficiency of ATP synthesis.

  2. the MT-ND1 gene is a hot spot for mutations associated with LHON.

  3. ND1 genetic polymorphisms associated with breast cancer in Mizoram mongloid population.

  4. The present study revealed no association between MS and T4216C variation in the ND1 mtDNA gene in the Iranian population.

  5. ND1 T3866C mutation is associated with Chinese families with Leber's hereditary optic neuropathy.

  6. 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.

  7. 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 ELISA试剂盒) mutations induced a severe structural and functional CI alteration.

  8. Novel mutations m.3959G>A and m.3995A>G in mitochondrial gene MT-ND1 associated with MELAS.

  9. 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.

  10. 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.

Mitochondrially Encoded NADH Dehydrogenase 1 (MT-ND1) 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-ND1

  • mitochondrial NADH-ubiquinone oxidoreductase chain 1 (mt:ND1) 抗体
  • NADH dehydrogenase, subunit 1 (complex I) (ND1) 抗体
  • NADH dehydrogenase subunit 1 (ND1) 抗体
  • NADH dehydrogenasesubunit 1 (nad1) 抗体
  • peptidylprolyl isomerase A (PPIA) 抗体
  • cypA 抗体
  • MT-ND1 抗体
  • MTND1 抗体
  • NADH1 抗体
  • ND1 抗体

Protein level used designations for MT-ND1

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

GENE ID SPECIES
192473 Drosophila melanogaster
4535 Homo sapiens
26193 Rattus norvegicus
17716 Mus musculus
804476 Canis lupus familiaris
807636 Gallus gallus
808501 Sus scrofa
808226 Oryctolagus cuniculus
808212 Branchiostoma lanceolatum
807667 Ascaris suum
807966 Locusta migratoria
1734038 Acanthamoeba castellanii
493966 Felis catus
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