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LOXL1 anticorps

Cet anticorps anti-LOXL1 est un anticorps Lapin Polyclonal détectant LOXL1 dans IF. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7255189

Aperçu rapide pour LOXL1 anticorps (ABIN7255189)

Antigène

Voir toutes LOXL1 Anticorps
LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

Reactivité

  • 48
  • 18
  • 7
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 49
  • 6
Lapin

Clonalité

  • 51
  • 4
Polyclonal

Conjugué

  • 26
  • 10
  • 9
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp LOXL1 est non-conjugé

Application

  • 36
  • 18
  • 15
  • 9
  • 8
  • 7
  • 3
  • 1
  • 1
Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

    Autre désignation

    LOXL1

    Sujet

    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.

    ID gène

    4016

    UniProt

    Q08397
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