NDUFA5 (Human) Matched Antibody Pair

Catalog # H00004698-AP21

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Size:1 Set
Price: USD $ 607.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human NDUFA5.

    Reactivity

    Human

    Quality Control Testing

    Standard curve using recombinant protein ( H00004698-P01 ) as an analyte.

    Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: rabbit MaxPab® affinity purified polyclonal anti-NDUFA5 (100 ug)
    2. Detection antibody: mouse polyclonal anti-NDUFA5 (40 ul)
    *Reagents are sufficient for at least 3-5 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Recombinant protein)

  • Gene Info — NDUFA5

    Entrez GeneID

    4698

    Gene Name

    NDUFA5

    Gene Alias

    B13, CI-13KD-B, DKFZp781K1356, FLJ12147, NUFM, UQOR13

    Gene Description

    NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5, 13kDa

    Omim ID

    601677

    Gene Ontology

    Hyperlink

    Gene Summary

    The human NDUFA5 gene codes for the B13 subunit of complex I of the respiratory chain, which transfers electrons from NADH to ubiquinone. The high degree of conservation of NDUFA5 extending to plants and fungi indicates its functional significance in the enzyme complex. The protein localizes to the inner mitochondrial membrane as part of the 7 component-containing, water soluble "iron-sulfur protein" (IP) fraction of complex I, although its specific role is unknown. It is assumed to undergo post-translational removal of the initiator methionine and N-acetylation of the next amino acid. The predicted secondary structure is primarily alpha helix, but the carboxy-terminal half of the protein has high potential to adopt a coiled-coil form. The amino-terminal part contains a putative beta sheet rich in hydrophobic amino acids that may serve as mitochondrial import signal. Related pseudogenes have also been identified on four other chromosomes. [provided by RefSeq

    Other Designations

    Complex I-13KD-B|NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5|NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 5 (13kD, B13)|type I dehydrogenase|ubiquinone reductase

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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