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Recombinant Human NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12 (NDUFA12)

ACP03173

Number
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Specifications


Cat.No ACP03173 Target NameNDUFA12
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range1-145aaMol Weight44.1kDa
Protein LengthFull lengthPurityGreater than 90% as determined by 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 IDQ9UI09
Background Information
  • Uniprot Id

    Q9UI09

  • Target Species

    Human

  • Target Name

    NDUFA12

  • Target Full Name

    NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12

  • 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 inner membrane; Peripheral membrane protein; Matrix side.

  • Target Protein Families

    Complex I NDUFA12 subunit family

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    13 kDa differentiation associated protein ; 13 kDa differentiation-associated protein; 2410011G03Rik; AW112974; B17.2; CI-B17.2; CIB17.2; Complex I B17.2; Complex I B17.2 subunit; Complex I-B17.2; DAP13; MGC107642; MGC7999; NADH dehydrogenase (ubiquinone) 1 alpha subcomplex 12; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12; NADH ubiquinone oxidoreductase subunit B17.2; NADH-ubiquinone oxidoreductase subunit B17.2; NDUAC_HUMAN; NDUFA12; RGD1311462

  • Target Background

    This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants.

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