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Coagulation Factor IX anticorps

F9 Reactivité: Humain, Souris, Rat WB, IHC (p), IF (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1387087
  • Antigène Voir toutes Coagulation Factor IX (F9) Anticorps
    Coagulation Factor IX (F9)
    Reactivité
    • 87
    • 33
    • 28
    • 5
    • 3
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 65
    • 15
    • 9
    • 8
    • 3
    • 1
    • 1
    Lapin
    Clonalité
    • 86
    • 15
    Polyclonal
    Conjugué
    • 51
    • 13
    • 8
    • 7
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Coagulation Factor IX est non-conjugé
    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))
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human Coagulation factor IXa heavy chain
    Isotype
    IgG
    Top Product
    Discover our top product F9 Anticorps primaire
  • Indications d'application
    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.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    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." dans: PLoS ONE, Vol. 12, Issue 7, pp. e0181634, (2017) (PubMed).

  • Antigène
    Coagulation Factor IX (F9)
    Autre désignation
    Factor 9 (F9 Produits)
    Synonymes
    anticorps AA407498, anticorps AI506714, anticorps AK-3, anticorps Ak3l, anticorps Ak3l1, anticorps Akl3l, anticorps FIX, anticorps HEMB, anticorps P19, anticorps PTC, anticorps THPH8, anticorps AW111646, anticorps Cf-9, anticorps Cf9, anticorps f9, anticorps zgc:109775, anticorps fix, anticorps ptc, anticorps hemb, anticorps FIXA, anticorps zgc:136807, anticorps adenylate kinase 3, anticorps coagulation factor IX, anticorps coagulation factor IXa, anticorps coagulation factor 9, anticorps coagulation factor 9 S homeolog, anticorps Coagulation factor IX, anticorps coagulation factor IXb, anticorps Ak3, anticorps F9, anticorps f9a, anticorps f9, anticorps CpipJ_CPIJ003776, anticorps CpipJ_CPIJ009129, anticorps CpipJ_CPIJ013063, anticorps CpipJ_CPIJ013624, anticorps Tsp_01441, anticorps f9.S, anticorps fa9, anticorps f9b
    Sujet

    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).

    ID gène
    2158
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