NDUFAF3 Antibodies

AND NDUFAF3 ELISA kits, NDUFAF3 Proteins

Many biological assays use antibodies to detect NDUFAF3, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NDUFAF3 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NDUFAF3 antibodies...

We validate the specificity of these antibodies to NDUFAF3 by testing them on tissues known to express NDUFAF3 positively and negatively. Browse below to find the NDUFAF3 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: SEPTIN9 Next: THUMPD3

NDUFAF3 Infographic by Boster Bio

All NDUFAF3 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

NDUF3 (NDUFAF3) (NM_199074) Human Recombinant Protein

$813
Cat # PROTQ9BU61
20 µg

NDUF3 (NDUFAF3) (NM_199069) Human Over-expression Lysate

Human

$628
Cat # LS025915
100 µg

NDUFAF3 Overview

Facts about NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3.

NDUFAF3 3D structure. Source: alphafold

NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3 (NDUFAF3)

Essential element for the assembly of mitochondrial NADH:ubiquinone oxidoreductase complex (complex I). .

Gene Information

Human
Gene Name:	NDUFAF3
Uniprot:	Q9BU61
Entrez:	25915

Family

Belongs to:

No superfamily

Alternative Names

C3orf60; chromosome 3 open reading frame 60; DKFZp564J0123; DKFZP564J0123,2P1; E3-3; MGC10527; NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 3; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3; nuclear protein E3-3

Molecular Weight

Mass (kDA):
20.35 kDA

Genomic Context


Human

Location:	3p21.31
Sequence:	3; NC_000003.12 (49020475..49023495)

Subcellular Localizations

Nucleus. Mitochondrion inner membrane.

Diseases

Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency
Mitochondrial Diseases
Trematode Infections

Interacting Proteins

NDUFAF4
RBCK1
REL
SNRPA

Pathways

Oxidative Phosphorylation
Spermatogenesis
Translation
Proteolysis
Pathogenesis
Iron-sulfur Cluster Assembly

PTMs

Phosphorylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NDUFAF3

References

PMID: 19463981 by Saada A., et al. Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)- interacting complex I assembly protein, cause fatal neonatal mitochondrial disease.

PMID: 27986404 by Baertling F., et al. Mutations in mitochondrial complex I assembly factor NDUFAF3 cause Leigh syndrome.