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Coagulation Factor IX antibody

F9 Reactivity: Human, Mouse, Rat WB, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7258664
  • Target See all Coagulation Factor IX (F9) Antibodies
    Coagulation Factor IX (F9)
    Reactivity
    • 87
    • 33
    • 28
    • 5
    • 3
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 65
    • 15
    • 9
    • 8
    • 3
    • 1
    • 1
    Rabbit
    Clonality
    • 85
    • 16
    Polyclonal
    Conjugate
    • 51
    • 13
    • 8
    • 7
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Coagulation Factor IX antibody is un-conjugated
    Application
    • 74
    • 45
    • 25
    • 13
    • 9
    • 8
    • 8
    • 8
    • 7
    • 7
    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human Factor IX / F9 (NP_000124.1).
    Isotype
    IgG
    Top Product
    Discover our top product F9 Primary Antibody
  • Application Notes
    WB 1:500-1:2000 IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: 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
    Coagulation Factor IX (F9)
    Alternative Name
    Factor IX / F9 (F9 Products)
    Background
    This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.
    Molecular Weight

    Observed_MW: 50 kDa

    Calculated_MW: 47 kDa/51 kDa

    Gene ID
    2158
    UniProt
    P00740
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