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NDUFA12 Protein (Myc-DYKDDDDK Tag)

NDUFA12 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2719206
  • Target See all NDUFA12 Proteins
    NDUFA12 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 12 (NDUFA12))
    Protein Type
    Recombinant
    Origin
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This NDUFA12 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human DAP13 / NDUFA12 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product NDUFA12 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    NDUFA12 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 12 (NDUFA12))
    Alternative Name
    Dap13,ndufa12 (NDUFA12 Products)
    Synonyms
    RGD1311462 Protein, si:dkey-183c16.3 Protein, zgc:112053 Protein, B17.2 Protein, DAP13 Protein, 2410011G03Rik Protein, AW112974 Protein, NADH:ubiquinone oxidoreductase subunit A12 Protein, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12 Protein, Ndufa12 Protein, NDUFA12 Protein, ndufa12 Protein
    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.
    Molecular Weight
    16.9 kDa
    NCBI Accession
    NP_061326
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