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VWF anticorps (Biotin)

Cet anticorps anti-VWF est un anticorps Human Chimeric détectant VWF dans FACS. Adapté pour Humain.
N° du produit ABIN7608408

Aperçu rapide pour VWF anticorps (Biotin) (ABIN7608408)

Antigène

Voir toutes VWF Anticorps
VWF (Von Willebrand Factor (VWF))

Reactivité

  • 191
  • 38
  • 28
  • 7
  • 6
  • 5
  • 1
  • 1
Humain

Hôte

  • 106
  • 104
  • 13
  • 7
  • 1
  • 1
Human, Lapin

Clonalité

  • 129
  • 100
  • 1
Chimeric

Conjugué

  • 105
  • 24
  • 15
  • 7
  • 7
  • 7
  • 7
  • 7
  • 7
  • 7
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp VWF est conjugé à/à la Biotin

Application

  • 140
  • 139
  • 76
  • 61
  • 57
  • 46
  • 31
  • 28
  • 25
  • 16
  • 16
  • 15
  • 9
  • 9
  • 7
  • 6
  • 6
  • 5
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
Flow Cytometry (FACS)

Clone

DMC389
  • Fonction

    Biotinylated Anti-VWF antibody(DMC389), IgG1 Chimeric mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG1
  • Indications d'application

    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

    VWF (Von Willebrand Factor (VWF))

    Autre désignation

    VWF

    Sujet

    This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22.

    UniProt

    P04275
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