NDUFA10 Antibodies

AND NDUFA10 ELISA kits, NDUFA10 Proteins

Many biological assays use antibodies to detect NDUFA10, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NDUFA10 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NDUFA10 antibodies...

We validate the specificity of these antibodies to NDUFA10 by testing them on tissues known to express NDUFA10 positively and negatively. Browse below to find the NDUFA10 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.

Designing a Western blot for NDUFA10? The guide has the expected band size, antibodies backed by real blot images, the controls to run alongside, and protocols taken from published papers.

Open the NDUFA10 Western Blot Guide

NDUFA10 Infographic by Boster Bio

All NDUFA10 Products

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Applications

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Anti-NDUFA10 Antibody Picoband®

Western blot analysis of NDUFA10 using anti-NDUFA10 antibody (A10517-1)

IHC analysis of NDUFA10 using anti-NDUFA10 antibody (A10517-1)

Human, Rat

ELISA, Flow Cytometry, IF, IHC, WB

$370
Cat # A10517-1
100 μg/vial

NDUFA10 (NM_004544) Human Over-expression Lysate

Human

$628
Cat # LS004705
20 µg, 100 µg

NDUFA10 Overview

Facts about NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial.

NDUFA10 3D structure. Source: alphafold

NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial (NDUFA10)

Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain.

The immediate electron acceptor for the enzyme is believed to be ubiquinone. .

Gene Information

Human
Gene Name:	NDUFA10
Uniprot:	O95299
Entrez:	4705

Family

Belongs to:

complex I NDUFA10 subunit family

Alternative Names

10 (42kD); CI-42k; CI-42KD; FLJ21923; MGC5103; NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 10, 42kDa; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial

Molecular Weight

Mass (kDA):
40.751 kDA

Genomic Context


Human

Location:	2q37.3
Sequence:	2; NC_000002.12 (239892442..240025402, complement)

Subcellular Localizations

Mitochondrion matrix.

Diseases

Cardiac Hypertrophy
Hypertrophy
Nerve Damage
Mitochondrial Diseases
Schizophrenia
Leigh Disease
Diabetes Mellitus
Diabetes Mellitus, Non-insulin-dependent

Hypertensive Disease
Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency
Fibrosis

Pathways

Oxidative Phosphorylation
Transport
Programmed Cell Death
Electron Transport
Insulin Secretion
Electron Transport Chain
Dna Methylation
Methylation
Flight
Respiratory Electron Transport Chain

Swimming
Cell Death
Pathogenesis
Secretion

PTMs

Phosphorylation

Oxidation

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NDUFA10

References

PMID: 9878551 by Loeffen J.L.C.M., et al. cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.

PMID: 21150889 by Hoefs S.J., et al. NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease.