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Fibrinogen beta Chain anticorps

L’anticorps Lapin Polyclonal anti-Fibrinogen beta Chain a été validé pour WB et ELISA. Il convient pour détecter Fibrinogen beta Chain dans des échantillons de Humain, Rat et Souris.
N° du produit ABIN7241348

Aperçu rapide pour Fibrinogen beta Chain anticorps (ABIN7241348)

Antigène

Voir toutes Fibrinogen beta Chain (FGB) Anticorps
Fibrinogen beta Chain (FGB)

Reactivité

  • 70
  • 16
  • 12
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 64
  • 20
  • 1
Lapin

Clonalité

  • 59
  • 26
Polyclonal

Conjugué

  • 46
  • 16
  • 9
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp Fibrinogen beta Chain est non-conjugé

Application

  • 60
  • 37
  • 24
  • 22
  • 10
  • 9
  • 8
  • 8
  • 6
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human FGB

    Isotype

    IgG
  • Indications d'application

    WB 1:1000-1:5000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.4 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    Fibrinogen beta Chain (FGB)

    Autre désignation

    FGB

    Sujet

    The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including afibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia and thrombotic tendency.

    Poids moléculaire

    56 kDa

    UniProt

    P02675
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