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Rabbit anti-Human NDUFA10 Polyclonal Antibody

The antibody against NDUFA10 was raised in rabbit using the Fusion protein of Human NDUFA10 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

ADC-29637A

The antibody against NDUFA10 was raised in rabbit using the Fusion protein of Human NDUFA10 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$299.00

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Specifications


Cat.No ADC-29637A ClonalityPolyclonal
Host SpeciesRabbitTarget NameNDUFA10
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.05% NaN3, 40% Glycerol., pH7.4 PBS
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionFusion protein of Human NDUFA10Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDO95299
Background Information
  • Uniprot Id

    O95299

  • Target Species

    Human

  • Target Name

    NDUFA10

  • Target Full Name

    NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial

  • Target Function

    Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in 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.

  • Target Involvement

    Leigh syndrome (LS)

  • Target Subcellular Location

    Mitochondrion matrix.

  • Target Protein Families

    Complex I NDUFA10 subunit family

  • Target Synonyms

    NDUFA10; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10; mitochondrial; Complex I-42kD; CI-42kD; NADH-ubiquinone oxidoreductase 42 kDa subunit

  • Target Background

    The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome.

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