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COX3 antibody (PE)

This anti-COX3 antibody is a Rabbit Polyclonal antibody detecting COX3 in WB. Suitable for Mouse, Rat and Human.
Catalog No. ABIN2173359

Quick Overview for COX3 antibody (PE) (ABIN2173359)

Target

See all COX3 (COX-3) Antibodies
COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

Reactivity

Mouse, Rat, Human

Host

  • 34
  • 2
Rabbit

Clonality

  • 34
  • 2
Polyclonal

Conjugate

  • 15
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This COX3 antibody is conjugated to PE

Application

  • 34
  • 13
  • 13
  • 13
  • 4
  • 4
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB)
  • 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 Notes

    FCM: (1:20-100)
    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • 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.
  • Target

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

    Alternative Name

    Cox3

    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
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