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Dynamin 1-Like Antikörper

DNM1L Reaktivität: Human, Maus, Ratte WB, IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7259550
  • Target Alle Dynamin 1-Like (DNM1L) Antikörper anzeigen
    Dynamin 1-Like (DNM1L)
    Reaktivität
    • 52
    • 45
    • 28
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 59
    • 8
    Kaninchen
    Klonalität
    • 59
    • 8
    Polyklonal
    Konjugat
    • 33
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Dynamin 1-Like Antikörper ist unkonjugiert
    Applikation
    • 34
    • 28
    • 18
    • 13
    • 13
    • 12
    • 9
    • 9
    • 4
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunofluorescence (IF)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human DRP1
    Isotyp
    IgG
    Top Product
    Discover our top product DNM1L Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000 IF 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Dynamin 1-Like (DNM1L)
    Andere Bezeichnung
    DRP1 (DNM1L Produkte)
    Hintergrund
    This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.
    Molekulargewicht

    Observed_MW: 82 kDa

    Calculated_MW: 60 kDa/78 kDa/79 kDa/80 kDa/81 kDa/82 kDa/83 kDa

    Gen-ID
    10059
    UniProt
    O00429
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