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Coagulation Factor IX anticorps (AA 29-192)

F9 Reactivité: Humain WB, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN3022174
  • Antigène Voir toutes Coagulation Factor IX (F9) Anticorps
    Coagulation Factor IX (F9)
    Épitope
    • 7
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 29-192
    Reactivité
    • 78
    • 27
    • 24
    • 5
    • 3
    • 1
    • 1
    Humain
    Hôte
    • 60
    • 14
    • 10
    • 4
    • 3
    • 1
    • 1
    Lapin
    Clonalité
    • 78
    • 14
    Polyclonal
    Conjugué
    • 53
    • 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
    • 69
    • 40
    • 27
    • 13
    • 9
    • 9
    • 8
    • 7
    • 6
    • 6
    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Séquence
    TVFLDHENAN KILNRPKRYN SGKLEEFVQG NLERECMEEK CSFEEAREVF ENTERTTEFW KQYVDGDQCE SNPCLNGGSC KDDINSYECW CPFGFEGKNC ELDVTCNIKN GRCEQFCKNS ADNKVVCSCT EGYRLAENQK SCEPAVPFPC GRVSVSQTSK LTRA
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein containing a sequence corresponding to amino acids 29-192 of human Factor IX / F9 (NP_000124.1).
    Isotype
    IgG
    Top Product
    Discover our top product F9 Anticorps primaire
  • Indications d'application
    WB,1:500 - 1:2000,IF,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Conseil sur la manipulation
    Avoid freeze / thaw cycles
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Coagulation Factor IX (F9)
    Autre désignation
    F9 (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
    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.,F9,F9 p22,FIX,HEMB,P19,PTC,THPH8,F9p22,Immunology & Inflammation,Cell Intrinsic Innate Immunity Signaling Pathway,Cardiovascular,Blood,Coagulation,F9
    Poids moléculaire
    47 kDa/51 kDa
    ID gène
    2158
    UniProt
    P00740
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