COX15 Antibodies

AND COX15 ELISA kits, COX15 Proteins

Many biological assays use antibodies to detect COX15, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with COX15 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop COX15 antibodies...

We validate the specificity of these antibodies to COX15 by testing them on tissues known to express COX15 positively and negatively. Browse below to find the COX15 antibody that suites your experiment. We have 2 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: CDH12 Next: CPB1

COX15 Infographic by Boster Bio

All COX15 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-COX15 Antibody

Human, Mouse, Rat

$405
Cat # A07168
100ul

Anti-COX15 Antibody

Human, Mouse, Rat

ELISA, IHC

$380
Cat # A07168-1
100ul

COX15 Overview

Facts about Cytochrome c oxidase assembly protein COX15 homolog.

COX15 3D structure. Source: alphafold

Cytochrome c oxidase assembly protein COX15 homolog (COX15)

May be involved in the biosynthesis of heme A. .

Gene Information

Human
Gene Name:	COX15
Uniprot:	Q7KZN9
Entrez:	1355

Family

Belongs to:

COX15/CtaA family

Alternative Names

COX15 (yeast) homolog, cytochrome c oxidase assembly protein; COX15 homolog, cytochrome c oxidase assembly protein (yeast); cytochrome c oxidase assembly protein COX15 homolog; cytochrome c oxidase subunit 15; EC 1.4.4.2; EC 3.1.3.5

Molecular Weight

Mass (kDA):
46.03 kDA

Genomic Context


Human

Location:	10q24.2
Sequence:	10; NC_000010.11 (99694293..99732131, complement)

Tissue Specificity

Predominantly found in tissues characterized by high rates of oxidative phosphorylation (OxPhos), including muscle, heart, and brain.

Subcellular Localizations

Mitochondrion membrane; Multi-pass membrane protein.

Diseases

Cytochrome-c Oxidase Deficiency
Leigh Disease
Cardiomyopathies
Mitochondrial Diseases
Hypertrophic Cardiomyopathy
Hypertrophy
Obesity
Microphthalmos
Neurodegenerative Disorders
Lung Diseases
Lung Diseases, Obstructive
Chronic Obstructive Airway Disease
Myopathy

Disorders Of Porphyrin Metabolism
Multisystem Disorder
Microphthalmia, Syndromic 7
Complete Hearing Loss
Microcephaly
Acidosis
Anemia

Interacting Proteins

PRDX6

Pathways

Transport
Electron Transport
Electron Transport Chain
Proteolysis
Oxidative Phosphorylation
Fermentation
Cell Proliferation
S Phase
Aging

Cell Growth
Pathogenesis
Localization

PTMs

Hydroxylation
Farnesylation
Oxidation

Phosphorylation
Biotinylation
Glycosylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/COX15

References

PMID: 9878253 by Petruzzella V., et al. Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain.

PMID: 12474143 by Antonicka H., et al. Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy.