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

The protein encoded by COQ6 belongs to the ubiH/COQ6 family. Zusätzlich bieten wir Ihnen Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) Antikörper (56) und und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
COQ6 299195  
COQ6 217707 Q8R1S0
COQ6 51004 Q9Y2Z9
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Top Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) Proteine auf antikoerper-online.de

Showing 8 out of 8 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 30 bis 35 Tage
$5,465.26
Details
Escherichia coli (E. coli) Maus His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 30 bis 35 Tage
$5,465.26
Details
Escherichia coli (E. coli) Human His tag Validation with Western Blot 50 μg Anmelden zum Anzeigen Verfügbar
$284.90
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Wheat germ Human GST tag 2 μg Anmelden zum Anzeigen 11 bis 12 Tage
$338.33
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Hefe Rind (Kuh) His tag   1 mg Anmelden zum Anzeigen 60 bis 71 Tage
$3,322.00
Details
Hefe Yeast His tag   1 mg Anmelden zum Anzeigen 60 bis 71 Tage
$3,353.17
Details
Escherichia coli (E. coli) Human Unkonjugiert SDS-PAGE analysis of Human COQ6 Protein. 100 μg Anmelden zum Anzeigen 11 bis 18 Tage
$483.26
Details
Escherichia coli (E. coli) Ratte Unkonjugiert SDS-PAGE analysis of Rat COQ6 Protein. 100 μg Anmelden zum Anzeigen 11 bis 18 Tage
$625.39
Details

COQ6 Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Rat (Rattus)
Mouse (Murine)

Human ,
,

Weitere Proteine zu Coenzyme Q6 Homolog, Monooxygenase (S. Cerevisiae) (COQ6) Interaktionspartnern

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

  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 (zeige EIF2C2 Proteine) (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 Überblick

Protein Überblick

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.

Genbezeichner und Symbole assoziert mit COQ6

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

Bezeichner auf Proteinebene für COQ6

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

GENE ID SPEZIES
299195 Rattus norvegicus
217707 Mus musculus
511624 Bos taurus
51004 Homo sapiens
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