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The antibody against COQ9 was raised in rabbit using the Human COQ9 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC, IF.
The antibody against COQ9 was raised in rabbit using the Human COQ9 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC, IF.
$600.00
| Cat.No | ADC-53730A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | COQ9 |
| Form | Liquid | Species Reactivity | Human, Mouse, Rat |
| Isotype | IgG | Storage Buffer | 50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium Azide |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, IF, IHC, WB | Storage | Upon receipt |
| Immunogen Description | Human COQ9 | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | O75208 |
Uniprot Id
O75208
Target Species
Human
Target Name
COQ9
Target Full Name
Ubiquinone biosynthesis protein COQ9, mitochondrial
Target Function
Lipid-binding protein involved in the biosynthesis of coenzyme Q, also named ubiquinone, an essential lipid-soluble electron transporter for aerobic cellular respiration. Binds a phospholipid of at least 10 carbons in each acyl group. May be required to present its bound-lipid to COQ7.
Target Involvement
Coenzyme Q10 deficiency, primary, 5 (COQ10D5)
Target Subcellular Location
Mitochondrion.
Target Protein Families
COQ9 family
Target Synonyms
C16orf49; Chromosome 16 open reading frame 49; Coenzyme Q9 homolog (S. cerevisiae); Coenzyme Q9 homolog (yeast); COQ9; COQ9_HUMAN; HSPC326; mitochondrial; PSEC0129; Ubiquinone biosynthesis protein COQ9; Ubiquinone biosynthesis protein COQ9; mitochondrial
Target Background
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.
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