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COX3 antibody

COX-3 Reactivity: Human WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2459381
  • Target See all COX3 (COX-3) Antibodies
    COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))
    Reactivity
    • 21
    • 18
    • 18
    Human
    Host
    • 33
    • 2
    Rabbit
    Clonality
    • 33
    • 2
    Polyclonal
    Conjugate
    • 13
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This COX3 antibody is un-conjugated
    Application
    • 33
    • 13
    • 13
    • 13
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    Purification
    Antibody is purified by peptide affinity chromatography method.
    Immunogen
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human COX3.
    Top Product
    Discover our top product COX-3 Primary Antibody
  • Application Notes
    COX3 antibody can be used for detection of COX3 by ELISA at 1:1562500. COX3 antibody can be used for detection of COX3 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    Concentration
    1 mg/mL
    Buffer
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    Handling Advice
    As with any antibody avoid repeat freeze-thaw cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store COX3 antibody at -20 °C.
  • Target
    COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))
    Alternative Name
    COX3 (COX-3 Products)
    Background
    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.
    Molecular Weight
    29 kDa
    Gene ID
    4514
    NCBI Accession
    NP_536849
    UniProt
    P00414
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