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FGA antibody

FGA Reactivity: Human, Rat, Mouse IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7234498
  • Target See all FGA Antibodies
    FGA (Fibrinogen alpha Chain (FGA))
    Reactivity
    • 45
    • 35
    • 25
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Rat, Mouse
    Host
    • 62
    • 18
    • 2
    • 2
    Rabbit
    Clonality
    • 65
    • 19
    Polyclonal
    Conjugate
    • 44
    • 12
    • 9
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This FGA antibody is un-conjugated
    Application
    • 65
    • 27
    • 25
    • 13
    • 13
    • 10
    • 9
    • 9
    • 8
    • 5
    • 5
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen Affinity Purification
    Immunogen
    Recombinant Mouse Fibrinogen alpha chain protein
    Isotype
    IgG
    Top Product
    Discover our top product FGA Primary Antibody
  • Application Notes
    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
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FGA (Fibrinogen alpha Chain (FGA))
    Alternative Name
    FGA (FGA Products)
    Synonyms
    Fib2 antibody, ENSMUSG00000059807 antibody, Fib antibody, Ac1873 antibody, Fba5e antibody, fibrinogen alpha chain antibody, FGA antibody, Fga antibody, LOC698244 antibody
    Background
    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.
    Gene ID
    14161
    UniProt
    E9PV24
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