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Coagulation Factor IX antibody

F9 Reactivity: Human, Mouse, Rat WB, IHC (p), IF (p) Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1387087
  • 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
    • 86
    • 15
    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
    • 44
    • 26
    • 12
    • 9
    • 8
    • 8
    • 7
    • 7
    • 7
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Cross-Reactivity
    Human, Mouse, Rat
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human Coagulation factor IXa heavy chain
    Isotype
    IgG
    Top Product
    Discover our top product F9 Primary Antibody
  • Application Notes
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
    Storage Comment
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Expiry Date
    12 months
  • Yang, Bae, Jung, Park, Chung, Seok, Roh, Han, Oh, Sohn, Jeong, Cho: "Surface functionalization-specific binding of coagulation factors by zinc oxide nanoparticles delays coagulation time and reduces thrombin generation potential in vitro." in: PLoS ONE, Vol. 12, Issue 7, pp. e0181634, (2017) (PubMed).

  • Target
    Coagulation Factor IX (F9)
    Alternative Name
    Factor 9 (F9 Products)
    Synonyms
    AA407498 antibody, AI506714 antibody, AK-3 antibody, Ak3l antibody, Ak3l1 antibody, Akl3l antibody, FIX antibody, HEMB antibody, P19 antibody, PTC antibody, THPH8 antibody, AW111646 antibody, Cf-9 antibody, Cf9 antibody, f9 antibody, zgc:109775 antibody, fix antibody, ptc antibody, hemb antibody, FIXA antibody, zgc:136807 antibody, adenylate kinase 3 antibody, coagulation factor IX antibody, coagulation factor IXa antibody, coagulation factor 9 antibody, coagulation factor 9 S homeolog antibody, Coagulation factor IX antibody, coagulation factor IXb antibody, Ak3 antibody, F9 antibody, f9a antibody, f9 antibody, CpipJ_CPIJ003776 antibody, CpipJ_CPIJ009129 antibody, CpipJ_CPIJ013063 antibody, CpipJ_CPIJ013624 antibody, Tsp_01441 antibody, f9.S antibody, fa9 antibody, f9b antibody
    Background

    Synonyms: Christmas Disease, Christmas factor, Coagulant factor IX, Coagulation factor 9, Coagulation factor IX plasma thromboplastic component, Coagulation factor IX, Coagulation factor IXa heavy chain, F9, FA9_HUMAN, Factor 9, Factor IX Deficiency, Factor9, FactorIX, FIX, GLA domain, Haemophilia B, MGC129641, MGC129642, P19 antibody Plasma thromboplastic component, Plasma thromboplastin component, PTC, Truncated coagulation factor IX.

    Background: Hemostasis following tissue injury involves the deployment of essential plasma procoagulants (prothrombin, and factors X, IX, V, and VIII), which are involved in a blood coagulation cascade that leads to the formation of insoluble fibrin clots and the promotion of platelet aggregation (1-3). Coagulation factor IX (plasma thromboplastic component, F9, F.IX, HEMB) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor (3,4). Factor XIa mediated proteolytic cleavage of factor IX generates factor IXa, an active serine protease composed of a 145 amino acid light chain and a 236 amino acid catalytic heavy chain, linked through disulfide bonds (5). Genetic alterations at the Factor IX locus such as point mutations, insertions and deletions, can lead to hemophilia B, also known as Christmas disease (6).

    Gene ID
    2158
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