Anti-Cytochrome c oxidase subunit 4, mitochondrial antibody [1A12A12] (ab110272)

Overview

  • Product nameAnti-Cytochrome c oxidase subunit 4, mitochondrial antibody [1A12A12]
  • Description
    Mouse monoclonal [1A12A12] to Cytochrome c oxidase subunit 4, mitochondrial
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Saccharomyces cerevisiae
  • Immunogen

    Native Complex IV from S. cerevisiae.

  • Positive control
    • Mitochondria from yeast membrane extract
  • General notes

    Product was previously marketed under the MitoSciences sub-brand.

Properties

Applications

Our Abpromise guarantee covers the use of ab110272 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB Use a concentration of 1 µg/ml. Predicted molecular weight: 17 kDa.

Target

  • Sequence similaritiesBelongs to the cytochrome c oxidase subunit 5B family.
  • Cellular localizationMitochondrion inner membrane.
  • Information by UniProt
  • Database links
    • Alternative names
      • cox4 antibody
      • COX4 Cox4p antibody
      • COX4_YEAST antibody
      • Cox4p antibody
      • Cytochrome c oxidase polypeptide IV antibody
      • Cytochrome c oxidase subunit 4 antibody
      • mitochondrial antibody
      • MS420 antibody
      see all

    Anti-Cytochrome c oxidase subunit 4, mitochondrial antibody [1A12A12] images

    • Anti-Cytochrome c oxidase subunit 4, mitochondrial antibody [1A12A12] (ab110272) at 1 µg/ml + Mitochondria from yeast membrane extract at 20 µg

      Predicted band size : 17 kDa

    References for Anti-Cytochrome c oxidase subunit 4, mitochondrial antibody [1A12A12] (ab110272)

    This product has been referenced in:
    • Wang L  et al. Azurocidin-induced inhibition of oxygen metabolism in mitochondria is antagonized by heparin. Exp Ther Med 8:1473-1478 (2014). Read more (PubMed: 25289044) »
    • Di Bella D  et al. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet 42:313-21 (2010). Read more (PubMed: 20208537) »

    See all 5 Publications for this product

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    Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"