COQ9 Antibodies

AND COQ9 ELISA kits, COQ9 Proteins

Many biological assays use antibodies to detect COQ9, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with COQ9 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop COQ9 antibodies...

We validate the specificity of these antibodies to COQ9 by testing them on tissues known to express COQ9 positively and negatively. Browse below to find the COQ9 antibody that suites your experiment. We have 3 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

Previous: Septin9 Next: CCNL1

COQ9 Infographic by Boster Bio

All COQ9 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-COQ9 Antibody

Human

$405
Cat # A03669
100ul

COQ9 (NM_020312) Human Recombinant Protein

$813
Cat # PROTO75208
20 µg

COQ9 (NM_020312) Human Over-expression Lysate

Human

$628
Cat # LS057017
100 µg

COQ9 Overview

Facts about Ubiquinone biosynthesis protein COQ9, mitochondrial.

COQ9 3D structure. Source: alphafold

Ubiquinone biosynthesis protein COQ9, mitochondrial (COQ9)

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. .

Gene Information

Human
Gene Name:	COQ9
Uniprot:	O75208
Entrez:	57017

Family

Belongs to:

COQ9 family

Alternative Names

C16orf49DKFZp434K046; chromosome 16 open reading frame 49; coenzyme Q9 homolog (S. cerevisiae); coenzyme Q9 homolog (yeast); DKFZP434K046; ubiquinone biosynthesis protein COQ9, mitochondrial

Molecular Weight

Mass (kDA):
35.509 kDA

Genomic Context


Human

Location:	16q21
Sequence:	16; NC_000016.10 (57447479..57461270)

Subcellular Localizations

Mitochondrion.

Diseases

Mitochondrial Diseases
Congenital Dyserythropoietic Anemia
Neoplasms
Lymphoma
Riboflavin Deficiency
Chronic Lymphocytic Leukemia
Hypertrophic Cardiomyopathy
Neuroblastoma
Acidosis
Developmental Delay (disorder)
B-cell Lymphomas

Malignant Paraganglionic Neoplasm
Haploinsufficiency
Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency
Cardiomyopathies
Hypertrophy
Leukemia

Interacting Proteins

ACSF2
COQ5
COQ7
COQ8A

Pathways

Transport
Electron Transport
Electron Transport Chain
Cell Growth
Oxidative Phosphorylation
Riboflavin Transport

Localization

PTMs

Phosphorylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/COQ9

References

PMID: 19375058 by Duncan A.J., et al. A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.

PMID: 25339443 by Lohman D.C., et al. Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 to enable coenzyme Q biosynthesis.