NDUFB9 antibody

Catalog No. ABIN7268815

This Rabbit Monoclonal antibody specifically detects NDUFB9 in WB and IHC. It exhibits reactivity toward Human.

Quick Overview for NDUFB9 antibody (ABIN7268815)

Target: NDUFB9 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 9, 22kDa (NDUFB9))

Reactivity: Human

Host: Rabbit

Clonality: Monoclonal

Conjugate: This NDUFB9 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Product Details anti-NDUFB9 Antibody

Purpose: NDUFB9 Rabbit mAb

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Monoclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant protein of Human NDUFB9.

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for NDUFB9

Target: NDUFB9 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 9, 22kDa (NDUFB9))

Alternative Name: NDUFB9

Background: The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants.,NDUFB9,B22,CI-B22,LYRM3,UQOR22,Endocrine & Metabolism,Mitochondrial metabolism,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFB9

Molecular Weight: 21kDa

Gene ID: 4715

UniProt: Q9Y6M9

Pathways: Sensory Perception of Sound, SARS-CoV-2 Protein Interactome