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Lipoprotein Lipase anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement Lipoprotein Lipase dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN926449

Aperçu rapide pour Lipoprotein Lipase anticorps (C-Term) (ABIN926449)

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
  • 31
  • 27
  • 21
  • 14
  • 14
  • 13
  • 9
  • 8
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 16
    • 9
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    C-Term

    Purification

    Purified

    Immunogène

    LPL antibody was raised in rabbit using the C terminal of LPL as the immunogen
  • Indications d'application

    Optimal conditions should be determined by the investigator.

    Commentaires

    LPL Blocking Peptide, (ABIN940389), is also available for use as a blocking control in assays to test for specificity of this LPL antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Concentration

    Lot specific

    Buffer

    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Antigène

    Lipoprotein Lipase (LPL)

    Autre désignation

    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. Synonyms: Polyclonal LPL antibody, Anti-LPL antibody, lipoprotein lipase antibody, HDLCQ11 antibody, LIPD antibody.

    Pathways

    Lipid Metabolism
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