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Coagulation Factor IX anticorps

F9 Reactivité: Humain IHC (p), EIA, ID Hôte: Mouton Polyclonal unconjugated
N° du produit ABIN951595
  • Antigène Voir toutes Coagulation Factor IX (F9) Anticorps
    Coagulation Factor IX (F9)
    Reactivité
    • 78
    • 28
    • 24
    • 5
    • 3
    • 1
    • 1
    Humain
    Hôte
    • 61
    • 14
    • 9
    • 4
    • 3
    • 2
    • 1
    Mouton
    Clonalité
    • 78
    • 15
    Polyclonal
    Conjugué
    • 54
    • 12
    • 6
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Coagulation Factor IX est non-conjugé
    Application
    • 71
    • 41
    • 27
    • 13
    • 9
    • 8
    • 7
    • 7
    • 7
    • 6
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA), Immunodiffusion (ID)
    Specificité
    Recognizes Human Factor IX as demonstrated by Immunodiffusion. A single positive reactivity band was observed with Normal Human Plasma. No reaction was observed against Factor IX-deficient plasma.
    Réactivité croisée (Details)
    Species reactivity (tested):Human.
    Purification
    Ammonium Sulfate Precipitation
    Immunogène
    Human Factor IX purified from plasma.
    Isotype
    IgG
    Top Product
    Discover our top product F9 Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    10 mg/mL
    Buffer
    0.01 M HEPES, pH 7.4, 0.1 M Sodium Chloride and 50 % Glycerol.
    Agent conservateur
    Azide free
    Conseil sur la manipulation
    Avoid repeated freezing and thawing.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène
    Coagulation Factor IX (F9)
    Abstract
    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
    Coagulation Factor IX (F9) 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.Synonyms: Christmas factor, PTC, Plasma thromboplastin component
    ID gène
    2158
    NCBI Accession
    NP_000124
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