NDUFAF2 antibody (PE-Cy5)

Catalog No. ABIN717968

The Rabbit Polyclonal anti-NDUFAF2 antibody is suitable to detect NDUFAF2 in samples from Human, Mouse and Rat. It has been validated for WB.

Quick Overview for NDUFAF2 antibody (PE-Cy5) (ABIN717968)

Target: NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFAF2 antibody is conjugated to PE-Cy5

Application: Western Blotting (WB)

Product Details anti-NDUFAF2 Antibody (PE-Cy5)

Predicted Reactivity: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Mimitin

Isotype: IgG

Application Details

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for NDUFAF2

Target: NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))

Alternative Name: Mimitin

Background:

Synonyms: mitochondrial, B17.2 like, B17.2-like, B17.2L, MIMIT_HUMAN, Mimitin, Mimitin mitochondrial, MMTN, Myc induced mitochondrial protein, Myc-induced mitochondrial protein, NADH dehydrogenase ubiquinone 1 alpha subcomplex assembly factor 2, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, NDUFA12 like, NDUFA12 like protein, NDUFA12-like protein, NDUFA12L, NDUFAF2.

Background: NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency.

Molecular Weight: 20kDa

Pathways: SARS-CoV-2 Protein Interactome