Background:

This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone)| a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme| which is part of the coenzyme Q10 pathway| catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement.

Classification:

Primary antibody

Alternative names:

COQ2

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human COQ2

Concentration:

1 mg/ml

Molecular weight:

40810

Applications:

WB

Storage:

-20°C for 1 year

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