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Lipase A anticorps

Cet anticorps anti-Lipase A Monoclonal Souris (Clone 9G7F12-7G6D7) (ABIN3210008) détecte spécifiquement Lipase A dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN3210008
1.184,92 €
Plus frais de livraison 40,00 € et TVA
100 μL
Destination: France
Envoi sous 20 à 27 jours ouvrables

Aperçu rapide pour Lipase A anticorps (ABIN3210008)

Antigène

Voir toutes Lipase A (LIPA) Anticorps
Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

Reactivité

  • 33
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 28
  • 6
Souris

Clonalité

  • 29
  • 6
Monoclonal

Conjugué

  • 20
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Lipase A est non-conjugé

Application

  • 23
  • 15
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA

Clone

9G7F12-7G6D7
  • Purification

    Purified antibody.

    Immunogène

    LAL antibody was raised in Mouse using a purified recombinant fragment of LAL expressed in E. coli as the immunogen.

    Isotype

    IgG2a
  • Indications d'application

    ELISA: 1:10,000, WB: 1:500-1:2000,
    Optimal conditions should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    Lot specific

    Buffer

    Purified antibody supplied in PBS containing 0.03 % sodium azide.

    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.

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at 4 °C for short term storage. Store at -20 °C for long term storage.
  • Antigène

    Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

    Autre désignation

    LAL

    Sujet

    LAL functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides which are taken up by receptor-mediated endocytosis. An inherited deficiency or low activity of human lysosomal acid lipase results in the intralysosomal storage of the respective lipid substrates. So it is also responsible for the rare conditions of Wolman disease and cholesteryl ester storage disease (CESD). As the enzyme is synthesized by all nucleated cells, lipid-laden cells are found in all organs, particularly in liver, spleen, the adrenal and the hemopoietic system, and in the intestine as well as in the lymph nodes, lungs, testes, and ovaries. Synonyms: Monoclonal LAL antibody, Anti-LAL antibody, Lysosomal acid lipase antibody.
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