Coenzyme Q4 Homolog (S. Cerevisiae) Proteins (COQ4)

Coenzyme Q (CoQ) is a small lipophilic molecule that transports electrons between mitochondrial respiratory chain complexes and functions as a cofactor for mitochondrial enzymes. Additionally we are shipping COQ4 Antibodies (3) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
COQ4 51117 Q9Y3A0
COQ4 366013 Q4FZU1
COQ4 227683 Q8BGB8
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Top COQ4 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
$4,744.22
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
$4,744.22
Details
Wheat germ Human GST tag 2 μg Log in to see 11 to 12 Days
$338.33
Details
Yeast Cow His tag   1 mg Log in to see 60 to 71 Days
$2,244.00
Details
Yeast Rat His tag   1 mg Log in to see 60 to 71 Days
$2,597.83
Details
Yeast Xenopus tropicalis His tag   1 mg Log in to see 60 to 71 Days
$2,687.67
Details

COQ4 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Rat (Rattus)

Mouse (Murine)

More Proteins for Coenzyme Q4 Homolog (S. Cerevisiae) (COQ4) Interaction Partners

Human Coenzyme Q4 Homolog (S. Cerevisiae) (COQ4) interaction partners

  1. Three genes in our epilepsy cohort (COQ4, DNM1 (show DNM1 Proteins), and PURA (show PURA Proteins)), accounting for 14% (3/21) of all novel genetic etiologies identified in patients with epilepsy, were subsequently confirmed in independent publications.

  2. five recessive missense mutations in COQ4 segregating with lethal neonatal mitochondrial encephalomyopathy in four families of Ashkenzi Jews

  3. COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency.

  4. Haploinsufficiency in COQ4 resulted in reduced COQ4 expression, CoQ10 content and biosynthetic rate, and activities of respiratory chain complex II+III.

  5. Human ortholog of Saccharomyces cerevisiae COQ4 was cloned and characterized.

Mouse (Murine) Coenzyme Q4 Homolog (S. Cerevisiae) (COQ4) interaction partners

COQ4 Protein Profile

Protein Summary

Coenzyme Q (CoQ) is a small lipophilic molecule that transports electrons between mitochondrial respiratory chain complexes and functions as a cofactor for mitochondrial enzymes. COQ4 is an enzyme involved in CoQ biosynthesis (Casarin et al., 2008

Gene names and symbols associated with COQ4

  • coenzyme Q4 L homeolog (coq4.L)
  • coenzyme Q4 (COQ4)
  • coenzyme Q4 (Coq4)
  • coenzyme Q4 homolog (S. cerevisiae) (coq4)
  • coenzyme Q4-like protein (LOC732978)
  • A330041N06 protein
  • CGI-92 protein
  • D2Ertd97e protein
  • si:dkey-170o10.3 protein

Protein level used designations for COQ4

Coenzyme Q biosynthesis protein 4 homolog , ubiquinone biosynthesis protein COQ4 homolog, mitochondrial , coenzyme Q biosynthesis protein 4 homolog , EST-MNCb4625

GENE ID SPECIES
100127306 Xenopus laevis
51117 Homo sapiens
366013 Rattus norvegicus
511987 Bos taurus
100137123 Danio rerio
227683 Mus musculus
732978 Bombyx mori
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