COX3 Rabbit anti-Human, Polyclonal, Bioss

Rabbit Polyclonal Antibody

Supplier:  Bioss BS3934R

Catalog No. 50-198-5767

Description

COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.

Specifications

• Antigen: COX3
• Classification: Polyclonal
• Conjugate: Unconjugated
• Gene: MT-CO3
• Gene Alias: ACI60_gp01; Co3; Coiii; COX3; COXIII; cytchrome c oxidase sububnit 3; Cytochrome c oxidase polypeptide III; Cytochrome c oxidase subunit 3; cytochrome c oxidase subunit III; mitochondrially encoded cytochrome c oxidase III; MTCO3; mt-Co3; OXI2; Q0275
• Host Species: Rabbit
• Purification Method: Protein A
• Regulatory Status: RUO
• Gene ID (Entrez): 139542, 4514
• Content And Storage: -20°C
• Form: Liquid

• Applications: Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
• Concentration: 1 μg/mL
• Formulation: PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
• Gene Accession No.: P00414
• Gene Symbols: COX3, MT-CO3
• Immunogen: KLH conjugated synthetic peptide derived from human COX3.
• Quantity: 100 μL
• Primary or Secondary: Primary
• Target Species: Human
• Product Type: Antibody
• Isotype: IgG