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PINK1 anticorps (Center)

L’anticorps Lapin Polyclonal anti-PINK1 a été validé pour . Il convient pour détecter PINK1 dans des échantillons de Humain et Souris.
N° du produit ABIN6295262

Aperçu rapide pour PINK1 anticorps (Center) (ABIN6295262)

Antigène

Voir toutes PINK1 Anticorps
PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

Reactivité

  • 82
  • 27
  • 10
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 55
  • 35
  • 1
Lapin

Clonalité

  • 59
  • 34
Polyclonal

Conjugué

  • 51
  • 8
  • 6
  • 5
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PINK1 est non-conjugé

Application

Veuillez nous consulter SVP
  • Épitope

    • 22
    • 8
    • 7
    • 6
    • 6
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 237-266, Center

    Fonction

    Rabbit Anti-PINK1 (PARK6) (Center) Antibody

    Immunogène

    This PINK1 (PARK6) antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 237-266 amino acids from the Central region of human PINK1 (PARK6).
  • Restrictions

    For Research Use only
  • Stock

    4 °C,-20 °C

    Stockage commentaire

    2-8°C (short-term), -20°C (long-term)
  • Antigène

    PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

    Autre désignation

    PINK1

    Sujet

    Target Description: Parkinson is the second most common neurodegenerative disease after Alzheimers. About 1 percent of people over the age of 65 and 3 percent of people over the age of 75 are affected by the disease. The mutation is the most common cause of Parkinson disease identified to date. Defects in PINK1 are the cause of autosomal recessive early-onset Parkinson's disease 6 (PARK6). Six novel pathogenic PINK1 mutations suggest that PINK1 may be the second most common causative gene next to parkin in parkinsonism with the recessive mode of inheritance. Strong evidence indicates that, although important in mendelian forms of Parkinson's disease (PD), PINK1 does not influence the cause of sporadic nonmendelian forms of PD.

    Gene Symbol: PINK1

    ID gène

    65018

    UniProt

    Q9BXM7

    Pathways

    Autophagy
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