Overview

  • Product name
  • Description
    Rabbit polyclonal to COQ9
  • Host species
    Rabbit
  • Tested applications
    Suitable for: WBmore details
  • Species reactivity
    Reacts with: Mouse, Human
  • Immunogen

    Synthetic peptide conjugated to KLH, corresponding to a region within internal sequence amino acids 160-190 of Human COQ9

  • Positive control
    • Mouse heart tissue lysates

Properties

Applications

Our Abpromise guarantee covers the use of ab104189 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 1/100 - 1/500. Predicted molecular weight: 35 kDa.

Target

  • Function
    Involved in the biosynthesis of coenzyme Q.
  • Pathway
    Cofactor biosynthesis; ubiquinone biosynthesis.
  • Involvement in disease
    Coenzyme Q10 deficiency, primary, 5
  • Sequence similarities
    Belongs to the COQ9 family.
  • Cellular localization
    Mitochondrion.
  • Information by UniProt
  • Database links
  • Alternative names
    • C16orf49 antibody
    • Chromosome 16 open reading frame 49 antibody
    • Coenzyme Q9 homolog (S. cerevisiae) antibody
    • Coenzyme Q9 homolog (yeast) antibody
    • COQ9 antibody
    • COQ9_HUMAN antibody
    • HSPC326 antibody
    • mitochondrial antibody
    • PSEC0129 antibody
    • Ubiquinone biosynthesis protein COQ9 antibody
    • Ubiquinone biosynthesis protein COQ9, mitochondrial antibody
    see all

Images

  • Anti-COQ9 antibody (ab104189) at 1/100 dilution + Mouse heart tissue lysates at 35 µg

    Predicted band size: 35 kDa

References

This product has been referenced in:
  • Luna-Sánchez M  et al. The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene. EMBO Mol Med 7:670-87 (2015). WB ; Mouse . Read more (PubMed: 25802402) »
  • García-Corzo L  et al. Dysfunctional Coq9 protein causes predominant encephalomyopathy associated with CoQ deficiency. Hum Mol Genet 22:1233-48 (2013). Read more (PubMed: 23255162) »

See all 2 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"

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