Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

PINK1 Antikörper (Center)

Der Kaninchen Polyklonal Anti-PINK1-Antikörper wurde für validiert. Er ist geeignet, PINK1 in Proben von Human und Maus zu detektieren.
Produktnummer ABIN6295262

Kurzübersicht für PINK1 Antikörper (Center) (ABIN6295262)

Target

Alle PINK1 Antikörper anzeigen
PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

Reaktivität

  • 89
  • 28
  • 10
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Maus

Wirt

  • 57
  • 44
  • 1
Kaninchen

Klonalität

  • 61
  • 43
Polyklonal

Konjugat

  • 58
  • 8
  • 6
  • 5
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser PINK1 Antikörper ist unkonjugiert

Applikation

Bitte anfragen
  • Bindungsspezifität

    • 28
    • 8
    • 7
    • 6
    • 6
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 237-266, Center

    Verwendungszweck

    Rabbit Anti-PINK1 (PARK6) (Center) Antibody

    Immunogen

    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).
  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

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

    PINK1 (PTEN Induced Putative Kinase 1 (PINK1))

    Andere Bezeichnung

    PINK1

    Hintergrund

    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

    Gen-ID

    65018

    UniProt

    Q9BXM7

    Pathways

    Autophagie
Sie sind hier:
Chat with us!