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COX3 anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement COX3 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN635599

Aperçu rapide pour COX3 anticorps (C-Term) (ABIN635599)

Antigène

Voir toutes COX3 (COX-3) Anticorps
COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

Reactivité

  • 22
  • 18
  • 17
Humain

Hôte

  • 33
  • 2
Lapin

Clonalité

  • 33
  • 2
Polyclonal

Conjugué

  • 13
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp COX3 est non-conjugé

Application

  • 33
  • 13
  • 13
  • 13
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 9
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Specificité

    COX3 antibody was raised against the C terminal of COX3

    Purification

    Affinity purified

    Immunogène

    COX3 antibody was raised using the C terminal of COX3 corresponding to a region with amino acids FESPFTISDGIYGSTFFVATGFHGLHVIIGSTFLTICFIRQLMFHFTSKH
  • Indications d'application

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Commentaires

    COX3 Blocking Peptide, (ABIN938266), is also available for use as a blocking control in assays to test for specificity of this COX3 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of COX3 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Antigène

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

    Autre désignation

    COX3

    Sujet

    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.

    Poids moléculaire

    29 kDa (MW of target protein)
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