COX3 antibody (AA 25-130) (Biotin)

Catalog No. ABIN751365

Product Details anti-COX3 Antibody (Biotin)

Target: COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

Binding Specificity: AA 25-130

Reactivity: Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This COX3 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Cross-Reactivity: Mouse, Rat

Predicted Reactivity: Human,Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human COX3

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for COX3

Target: COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

Alternative Name: COX3 (COX-3 Products)

Synonyms: COIII antibody, MTCO3 antibody, cytochrome c oxidase III antibody, cytochrome c oxidase subunit III antibody, cytochrome c oxidase subunit 3 antibody, cytochrome oxidasesubunit 3 antibody, COX3 antibody, cox3 antibody

Background:

Synonyms: Cytochrome c oxidase polypeptide III, Cytochrome c oxidase subunit 3, COIII, COX3, COX-3, COXIII, MT CO3, MTCO3, COX3_HUMAN.

Background: Cytochrome C Oxidase subunits I, II and III form the functional core of the enzyme complex.Defects in Cytochrome C Oxidase subunits III are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in Cytochrome C Oxidase subunits III are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.

Gene ID: 4514