COA7 Antibodies

AND COA7 ELISA kits, COA7 Proteins

Many biological assays use antibodies to detect COA7, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with COA7 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop COA7 antibodies...

We validate the specificity of these antibodies to COA7 by testing them on tissues known to express COA7 positively and negatively. Browse below to find the COA7 antibody that suites your experiment. We have 1 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.

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COA7 Infographic by Boster Bio

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C1orf163 (COA7) (NM_023077) Human Over-expression Lysate

Human

$628
Cat # LS065260
100 µg

COA7 Overview

Facts about Cytochrome c oxidase assembly factor 7.

COA7 3D structure. Source: alphafold

Cytochrome c oxidase assembly factor 7 (COA7)

Required for assembly of mitochondrial respiratory chain complex I and complex IV. .

Gene Information

Human
Gene Name:	COA7
Uniprot:	Q96BR5
Entrez:	65260

Family

Belongs to:

hcp beta-lactamase family

Alternative Names

Cytochrome c oxidase assembly factor 7

Molecular Weight

Mass (kDA):
25.709 kDA

Genomic Context


Human

Location:	1p32.3
Sequence:	1; NC_000001.11 (52684449..52698347, complement)

Subcellular Localizations

Mitochondrion intermembrane space. The import in the mitochondrion intermembrane space is mediated by CHCHD4/MIA40.

Diseases

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3 (SCAN3)

PTMs

Acetylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/COA7

References

PMID: 24333015 by Kozjak-Pavlovic V., et al. C1orf163/RESA1 is a novel mitochondrial intermembrane space protein connected to respiratory chain assembly.

PMID: 27683825 by Martinez Lyons A., et al. COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency.