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ANGPTL3 anticorps (Biotin)

Cet anticorps anti-ANGPTL3 est un anticorps Lapin Monoclonal détectant ANGPTL3 dans ELISA et FACS. Adapté pour Humain.
N° du produit ABIN7608045

Aperçu rapide pour ANGPTL3 anticorps (Biotin) (ABIN7608045)

Antigène

Voir toutes ANGPTL3 Anticorps
ANGPTL3 (Angiopoietin-Like 3 (ANGPTL3))

Reactivité

  • 62
  • 22
  • 14
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 51
  • 11
  • 3
  • 3
  • 1
Lapin

Clonalité

  • 52
  • 16
Monoclonal

Conjugué

  • 50
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp ANGPTL3 est conjugé à/à la Biotin

Application

  • 47
  • 29
  • 19
  • 10
  • 10
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
ELISA, Flow Cytometry (FACS)

Clone

DM205
  • Fonction

    Biotinylated Anti-ANGPTL3 antibody(DM205), Rabbit mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG
  • Indications d'application

    ELISA 1:5000-10000, Flow Cyt 1:100

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    Stock

    -20 °C,-80 °C

    Stockage commentaire

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Date de péremption

    12 months
  • Antigène

    ANGPTL3 (Angiopoietin-Like 3 (ANGPTL3))

    Autre désignation

    ANGPTL3

    Sujet

    This gene encodes a member of a family of secreted proteins that function in angiogenesis. The encoded protein, which is expressed predominantly in the liver, is further processed into an N-terminal coiled-coil domain-containing chain and a C-terminal fibrinogen chain. The N-terminal chain is important for lipid metabolism, while the C-terminal chain may be involved in angiogenesis. Mutations in this gene cause familial hypobetalipoproteinemia type 2.

    UniProt

    Q9Y5C1
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