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Coenzyme Q9 Homolog (S. Cerevisiae) Proteins (COQ9)

This locus represents a mitochondrial ubiquinone biosynthesis gene. Additionally we are shipping COQ9 Antibodies (28) and COQ9 Kits (1) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
COQ9 57017 O75208
COQ9 498909 Q68FT1
COQ9 67914 Q8K1Z0
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Top COQ9 Proteins at antibodies-online.com

Showing 5 out of 5 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
Yeast Rat His tag   1 mg Log in to see 56 to 66 Days
$2,693.17
Details
Yeast Cow His tag   1 mg Log in to see 56 to 66 Days
$2,715.17
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 9 to 11 Days
$785.40
Details

COQ9 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,

Rat (Rattus)

Mouse (Murine)

More Proteins for Coenzyme Q9 Homolog (S. Cerevisiae) (COQ9) Interaction Partners

Human Coenzyme Q9 Homolog (S. Cerevisiae) (COQ9) interaction partners

  1. Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 (show Coq7 Proteins) to enable coenzyme Q biosynthesis.

  2. There is a homozygous stop mutation affecting a highly conserved residue of COQ9, leading to the truncation of 75 amino acids.

Mouse (Murine) Coenzyme Q9 Homolog (S. Cerevisiae) (COQ9) interaction partners

  1. The presence of a truncated version of COQ9 protein in Coq9(R239X) mice destabilizes the coenzyme Q10 (show H2-Q10 Proteins)-synthesizing multiprotein complex.

  2. Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 (show Coq7 Proteins) to enable coenzyme Q biosynthesis.

  3. Lack of a functional Coq9 protein causes predominant encephalomyopathy and CoQ deficiency.

  4. Although Pdss2 (show PDSS2 Proteins) mutant mice manifest widespread CoQ(9) deficiency and mitochondrial respiratory chain abnormalities, only affected organs show increased ROS (show ROS1 Proteins) production, oxidative stress, mitochondrial DNA depletion, and reduced citrate synthase (show CS Proteins) activity.

COQ9 Protein Profile

Protein Summary

This locus represents a mitochondrial ubiquinone biosynthesis gene. The encoded protein is likely necessary for biosynthesis of coenzyme Q10, as mutations at this locus have been associated with autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency.

Gene names and symbols associated with COQ9

  • coenzyme Q9 homolog (S. cerevisiae) (COQ9)
  • coenzyme Q9 homolog (S. cerevisiae) (Coq9)
  • coenzyme Q9 homolog (yeast) (Coq9)
  • 2310005O14Rik protein
  • C16orf49 protein
  • C78387 protein
  • COQ10D5 protein

Protein level used designations for COQ9

ubiquinone biosynthesis protein COQ9, mitochondrial

GENE ID SPECIES
57017 Homo sapiens
498909 Rattus norvegicus
529282 Bos taurus
67914 Mus musculus
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