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Lipoprotein Lipase anticorps

LPL Reactivité: Humain, Rat, Souris IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7259018
  • Antigène Voir toutes Lipoprotein Lipase (LPL) Anticorps
    Lipoprotein Lipase (LPL)
    Reactivité
    • 72
    • 27
    • 21
    • 16
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 59
    • 17
    • 2
    Lapin
    Clonalité
    • 54
    • 25
    Polyclonal
    Conjugué
    • 35
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Lipoprotein Lipase est non-conjugé
    Application
    • 63
    • 33
    • 32
    • 23
    • 15
    • 14
    • 14
    • 8
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human LPL (NP_000228.1).
    Isotype
    IgG
    Top Product
    Discover our top product LPL Anticorps primaire
  • 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
    Lipoprotein Lipase (LPL)
    Autre désignation
    LPL (LPL Produits)
    Synonymes
    anticorps HDLCQ11, anticorps LIPD, anticorps fb62e04, anticorps fc49b03, anticorps wu:fb62e04, anticorps wu:fc49b03, anticorps LPL, anticorps lipd, anticorps hdlcq11, anticorps lpl, anticorps LOC100223817, anticorps lipoprotein lipase, anticorps LPL, anticorps Lpl, anticorps lpl
    Sujet
    LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism.
    ID gène
    4023
    UniProt
    P06858
    Pathways
    Lipid Metabolism
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