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LOXL1 Antikörper

Der Kaninchen Polyklonal Anti-LOXL1-Antikörper wurde für IF validiert. Er ist geeignet, LOXL1 in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN6566806

Kurzübersicht für LOXL1 Antikörper (ABIN6566806)

Target

Alle LOXL1 Antikörper anzeigen
LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

Reaktivität

  • 56
  • 22
  • 9
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Human, Maus, Ratte

Wirt

  • 60
  • 7
Kaninchen

Klonalität

  • 62
  • 5
Polyklonal

Konjugat

  • 36
  • 11
  • 10
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser LOXL1 Antikörper ist unkonjugiert

Applikation

  • 46
  • 26
  • 19
  • 18
  • 15
  • 9
  • 3
  • 1
  • 1
Immunofluorescence (IF)
  • Aufreinigung

    Affinity purification

    Immunogen

    Recombinant fusion protein of human LOXL1 (NP_005567.2).

    Isotyp

    IgG
  • Applikationshinweise

    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

    LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

    Andere Bezeichnung

    LOXL1

    Hintergrund

    This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome.

    Molekulargewicht

    Observed_MW: 80kDa

    Calculated_MW: 63kDa

    Gen-ID

    4016

    UniProt

    Q08397
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