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Recombinant Human NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3 (NDUFB3), Truncated

ACP06683

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP06683 Target NameNDUFB3
Target SynonymsNDUFB3; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3; Complex I-B12; CI-B12; NADH-ubiquinone oxidoreductase B12 subunitFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDO43676
Background Information
  • Uniprot Id

    O43676

  • Target Species

    Human

  • Target Name

    NDUFB3

  • Target Full Name

    NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3

  • 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

    Mitochondrial complex I deficiency (MT-C1D)

  • Target Subcellular Location

    Mitochondrion inner membrane; Single-pass membrane protein; Matrix side.

  • Target Protein Families

    Complex I NDUFB3 subunit family

  • Target Synonyms

    NDUFB3; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3; Complex I-B12; CI-B12; NADH-ubiquinone oxidoreductase B12 subunit

  • Target Background

    This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. This protein localizes to the inner membrane of the mitochondrion as a single-pass membrane protein. Mutations in this gene contribute to mitochondrial complex 1 deficiency. Alternative splicing results in multiple transcript variants encoding the same protein. Humans have multiple pseudogenes of this gene.

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