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FGA anticorps

FGA Reactivité: Humain, Rat, Souris IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7234498
  • Antigène Voir toutes FGA Anticorps
    FGA (Fibrinogen alpha Chain (FGA))
    Reactivité
    • 45
    • 35
    • 25
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 62
    • 18
    • 2
    • 2
    Lapin
    Clonalité
    • 65
    • 19
    Polyclonal
    Conjugué
    • 44
    • 12
    • 9
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FGA est non-conjugé
    Application
    • 65
    • 27
    • 25
    • 13
    • 13
    • 10
    • 9
    • 9
    • 8
    • 5
    • 5
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen Affinity Purification
    Immunogène
    Recombinant Mouse Fibrinogen alpha chain protein
    Isotype
    IgG
    Top Product
    Discover our top product FGA Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.65 mg/mL
    Buffer
    PBS with 0.05 % Proclin300, 50 % glycerol, pH 7.3
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: 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
    FGA (Fibrinogen alpha Chain (FGA))
    Autre désignation
    FGA (FGA Produits)
    Synonymes
    anticorps Fib2, anticorps ENSMUSG00000059807, anticorps Fib, anticorps Ac1873, anticorps Fba5e, anticorps fibrinogen alpha chain, anticorps FGA, anticorps Fga, anticorps LOC698244
    Sujet
    This gene encodes the alpha subunit of the coagulation factor fibrinogen, which is a component of the blood clot. Following vascular injury, the encoded preproprotein is proteolytically processed by thrombin during the conversion of fibrinogen to fibrin. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia, afibrinogenemia and renal amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that undergoes proteolytic processing.
    ID gène
    14161
    UniProt
    E9PV24
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