Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) Proteins (COQ6)

The protein encoded by COQ6 belongs to the ubiH/COQ6 family. Additionally we are shipping Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) Antibodies (48) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
Rat COQ6 COQ6 299195  
COQ6 217707 Q8R1S0
COQ6 51004 Q9Y2Z9
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) Proteins at antibodies-online.com

Showing 6 out of 6 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 30 to 35 Days
$4,331.68
Details
Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 30 to 35 Days
$4,331.68
Details
Escherichia coli (E. coli) Human His tag Validation with Western Blot 50 μg Log in to see 10 to 12 Days
$229.85
Details
Wheat germ Human GST tag 2 μg Log in to see 11 to 12 Days
$333.33
Details
Yeast Cow His tag   1 mg Log in to see 60 to 71 Days
$3,322.00
Details
Yeast Yeast His tag   1 mg Log in to see 60 to 71 Days
$3,353.17
Details

COQ6 Proteins by Origin and Source

Origin Expressed in Conjugate
Mouse (Murine)

Human ,
,

More Proteins for Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) (COQ6) Interaction Partners

Human Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) (COQ6) interaction partners

  1. Primary CoQ10 deficiency due to COQ6 mutations should be considered in children presenting with both Steroid-Resistant Focal Segmental Glomerulosclerosis and sensorineural hearing loss. An early diagnosis of COQ6 mutations is essential because the condition is treatable when CoQ10 supplementation is started at the early stage.

  2. Data indicate a heterozygous loss-of-function coenzyme Q10 (show EIF2C2 Proteins) (CoQ10) biosynthesis monooxygenase 6 gene (COQ6)missense mutation in familial schwannomatosis.

  3. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) (COQ6) Protein Profile

Protein Summary

The protein encoded by this gene belongs to the ubiH/COQ6 family. It is an evolutionarily conserved monooxygenase required for the biosynthesis of coenzyme Q10 (or ubiquinone), which is an essential component of the mitochondrial electron transport chain, and one of the most potent lipophilic antioxidants implicated in the protection of cell damage by reactive oxygen species. Knockdown of this gene in mouse and zebrafish results in decreased growth due to increased apoptosis. Mutations in this gene are associated with autosomal recessive coenzyme Q10 deficiency-6 (COQ10D6), which manifests as nephrotic syndrome with sensorineural deafness. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Gene names and symbols associated with COQ6

  • coenzyme Q6 monooxygenase (Coq6)
  • coenzyme Q6, monooxygenase (COQ6)
  • 5930427M12Rik protein
  • AW742344 protein
  • CGI10 protein
  • COQ10D6 protein

Protein level used designations for COQ6

ubiquinone biosynthesis monooxygenase COQ6 , coenzyme Q10 monooxygenase 6 , coenzyme Q6 homolog, monooxygenase

GENE ID SPECIES
299195 Rattus norvegicus
217707 Mus musculus
511624 Bos taurus
51004 Homo sapiens
Selected quality suppliers for Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) Proteins (COQ6)
Did you look for something else?