NDUFAF4 antibody (full length)

Catalog No. ABIN2856655

This Rabbit Polyclonal antibody specifically detects NDUFAF4 in WB. It exhibits reactivity toward Human.

Quick Overview for NDUFAF4 antibody (full length) (ABIN2856655)

Target: NDUFAF4 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 4 (NDUFAF4))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFAF4 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-NDUFAF4 Antibody

Binding Specificity: full length

Characteristics: Rabbit polyclonal antibody to HRPAP20 (chromosome 6 open reading frame 66)
HRPAP20 antibody [N1C3]

Purification: Purified by antigen-affinity chromatography.

Immunogen: Full length human HRPAP20 Recombinant protein.

Isotype: IgG

Application Details

Application Notes: Suggested dilution Reference Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceWestern blot1:500-1:3000*

Comment:

Positive Control: 293T , Raji

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for NDUFAF4

Target: NDUFAF4 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 4 (NDUFAF4))

Alternative Name: HRPAP20

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 are a cause of mitochondrial complex I deficiency.

Cellular Localization: Mitochondrion

Molecular Weight: 20 kDa

Gene ID: 29078