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Rabbit anti-Human MT-ND5 Polyclonal Antibody

The antibody against MT-ND5 was raised in rabbit using the Recombinant Human NADH-ubiquinone oxidoreductase chain 5 protein (503-581AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB.

ADC-07857A

The antibody against MT-ND5 was raised in rabbit using the Recombinant Human NADH-ubiquinone oxidoreductase chain 5 protein (503-581AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB.

$299.00

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Specifications


Cat.No ADC-07857A ClonalityPolyclonal
Host SpeciesRabbitTarget NameMT-ND5
Target SynonymsComplex I, subunit ND5 antibody; NADH ubiquinone oxidoreductase chain 5 antibody; NADH-ubiquinone oxidoreductase chain 5 antibody; NADH5 antibody; ND5 antibody; NU5M_HUMAN antibodyFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4Purification Method>95%, Protein G purified
ConjugateNon-conjugatedApplicationELISA, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human NADH-ubiquinone oxidoreductase chain 5 protein (503-581AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP03915
Background Information
  • Uniprot Id

    P03915

  • Target Species

    Human

  • Target Name

    MT-ND5

  • Target Full Name

    NADH-ubiquinone oxidoreductase chain 5

  • Target Function

    Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which catalyzes electron transfer from NADH through the respiratory chain, using ubiquinone as an electron acceptor. Essential for the catalytic activity and assembly of complex I.

  • Target Involvement

    Leber hereditary optic neuropathy (LHON); Leigh syndrome (LS); Mitochondrial complex I deficiency (MT-C1D); Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome (MELAS)

  • Target Subcellular Location

    Mitochondrion inner membrane; Multi-pass membrane protein.

  • Target Protein Families

    Complex I subunit 5 family

  • Target Synonyms

    Complex I, subunit ND5; EC 1.6.5.3; Mitochondrially encoded NADH dehydrogenase 5; MT ND5; MT-ND5; MTND 5; MTND5; NAD5; NADH dehydrogenase subunit 5 (complex I); NADH dehydrogenase subunit 5; NADH ubiquinone oxidoreductase , subunit ND5; NADH ubiquinone oxidoreductase chain 5; NADH-ubiquinone oxidoreductase chain 5; NADH5; ND5; NU5M_HUMAN

  • Target Background

    Contributes to NADH dehydrogenase (ubiquinone) activity. Predicted to be involved in electron transport coupled proton transport; mitochondrial electron transport, NADH to ubiquinone; and mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Is expressed in central nervous system; heart; liver; metanephros; and retina. Human ortholog(s) of this gene implicated in Leber hereditary optic neuropathy; Leigh disease; and MELAS syndrome. Orthologous to human MT-ND5 (mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5).

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