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Lipoprotein Lipase anticorps (Center)

Cet anticorps anti-Lipoprotein Lipase est un anticorps Lapin Polyclonal détectant Lipoprotein Lipase dans WB, IHC et FACS. Adapté pour Humain.
N° du produit ABIN2798466

Aperçu rapide pour Lipoprotein Lipase anticorps (Center) (ABIN2798466)

Antigène

Voir toutes Lipoprotein Lipase (LPL) Anticorps
Lipoprotein Lipase (LPL)

Reactivité

  • 85
  • 30
  • 24
  • 19
  • 6
  • 6
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 68
  • 25
  • 2
Lapin

Clonalité

  • 61
  • 34
  • 1
Polyclonal

Conjugué

  • 47
  • 8
  • 7
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Lipoprotein Lipase est non-conjugé

Application

  • 73
  • 37
  • 30
  • 26
  • 21
  • 14
  • 14
  • 13
  • 9
  • 8
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
  • Épitope

    • 16
    • 8
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 300-327, Center

    Fonction

    Rabbit Anti-Human LPL (Center) Antibody

    Immunogène

    This LPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 300-327 amino acids from the Central region of human LPL.

    Isotype

    Ig Fraction
  • Indications d'application

    Western Blot, Immunohistochemistry, Flow Cytometry
    Recommended Dilutions
    WB: 1:1000, IHC: 1:10-50, FC: 1:10-50LPL Antibody (Center) .FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Stock

    4 °C,-20 °C

    Stockage commentaire

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

    Lipoprotein Lipase (LPL)

    Autre désignation

    LPL

    Sujet

    Target Description: 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. [provided by RefSeq].

    Gene Symbol: LPL

    Poids moléculaire

    53162 Da

    ID gène

    4023

    UniProt

    P06858

    Pathways

    Lipid Metabolism
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